Gardner Denver biovac 106 with 2 L Container User manual

Operation Manual
(EN)
Translation of the german original manual
Aspiration Systems
Models:
►biovac 106
with 2 L Container
► biovac 106
with 4 L Container
112037
2017-04-10

We are constantly working on the further
development of all our product models.
Reprinting or reproduction of this manual,
including extracts, is not allowed without the
prior written permission of Co. Gardner Denver
Thomas GmbH.
All rights under the copyright laws are
expressly reserved by Co. Gardner Denver
Thomas GmbH.
We reserve the right to make changes and
amendments.
Gardner Denver Thomas GmbH
Am Vogelherd 20
98693 Ilmenau
Germany
T +49 3677 604 0
F +49 3677 604 131
welch.emea@gardnerdenver.com
www.welchvacuum.com
Customer Support +49 3677 604 0

Contents
112037 3
Contents
1Important Information........................................................................................................................... 4
1.1 General information ................................................................................................................................ 4
1.2 Target groups.......................................................................................................................................... 4
1.3 Intended Use........................................................................................................................................... 4
1.4 Use for an Unauthorized Purpose........................................................................................................... 4
1.5 Safety Devices........................................................................................................................................ 5
1.6 Meaning of the Warning notes................................................................................................................ 5
1.7 Product Standards, Safety Regulations .................................................................................................. 5
2Basic Safety Instructions..................................................................................................................... 6
2.1 General information ................................................................................................................................ 6
2.2 Electricity................................................................................................................................................. 6
2.3 Mechanical System................................................................................................................................. 6
2.4 Hazardous Substances........................................................................................................................... 7
2.5 High Temperatures ................................................................................................................................. 7
3Description............................................................................................................................................ 8
3.1 Design..................................................................................................................................................... 8
3.2 Function.................................................................................................................................................. 9
3.3 Materials of the medium-affecting pump parts...................................................................................... 10
3.4 Areas of Application.............................................................................................................................. 10
3.5 Possible Accessories............................................................................................................................ 10
3.6 Scope of Delivery.................................................................................................................................. 10
4Technical Data..................................................................................................................................... 11
4.1 Dimensions........................................................................................................................................... 11
4.2 Device Data .......................................................................................................................................... 12
4.3 Intake Pressure/Pumping Speed –Diagram......................................................................................... 12
5Installation and Operation.................................................................................................................. 13
5.1 Unpacking............................................................................................................................................. 13
5.2 Installation and Connection................................................................................................................... 13
5.2.1 Connection schematic –biovac 106 ..................................................................................................... 14
5.3 Operation.............................................................................................................................................. 14
5.4 Storage ................................................................................................................................................. 15
5.5 Scrap Disposal...................................................................................................................................... 15
6Maintenance and Servicing................................................................................................................ 16
6.1 General Requirements.......................................................................................................................... 16
6.2 Maintenance Performed by the User .................................................................................................... 16
6.2.1 Maintenance of the aspiration systems................................................................................................. 16
6.2.1.1 Disassembly.......................................................................................................................................... 16
6.2.1.2 Assembly .............................................................................................................................................. 17
6.2.1.3 Test....................................................................................................................................................... 17
6.2.2 Maintenance of the diaphragm pump.................................................................................................... 17
6.2.2.1 Disassembly.......................................................................................................................................... 17
6.2.2.2 Assembly .............................................................................................................................................. 18
6.2.2.3 Test....................................................................................................................................................... 18
6.2.3 Maintenance of other components........................................................................................................ 18
6.3 Maintenance by the Manufacturer......................................................................................................... 19
6.4 Damage Report..................................................................................................................................... 19
7Troubleshooting.................................................................................................................................. 20
8Spare Parts Overview......................................................................................................................... 21
8.1 Service kit - Diaphragm pump............................................................................................................... 21
8.2 Spare parts views ................................................................................................................................. 22
8.2.1 Complete unit - biovac 106 with secretion glass container 2 liters........................................................ 22
8.2.1.1 Spare parts list - Complete unit biovac 106 with secretion glass container 2 liters............................... 22
8.2.2 Complete unit - biovac 106 with secretion PP - container 4 liters ......................................................... 23
8.2.2.1 Spare parts list - Complete unit biovac 106 with secretion PP - container 4 liters................................. 23
8.2.3 Spare parts view - Basic unit complete................................................................................................. 24
8.2.3.1 Spare parts list - Basic unit complete.................................................................................................... 25
EC Declaration of Conformity

Important Information
4 112037
1 Important Information
1.1 General information
The biovac 106 Aspiration Systems conforms to the:
2006 / 42 / EC
Machinery Directive
2014/ 30 / EU
Electromagnetic Compatibility Directive
The CE sign is located on the rating plate. Observe the binding national and local regulations
when fitting the system into installations.
Our products are sold worldwide and can therefore be equipped with the typical national
plugs and for the various voltages. You will find more information about the available pump
designs on our web page in the internet.
1.2 Target groups
This Operating Manual is intended for the personnel planning, operating and maintaining the
biovac aspiration systems. This group of people includes:
Designers and fitters of vacuum apparatus,
Employees working on commercial laboratory and industrial vacuum technology applica-
tions and
Service personnel for biovac aspiration systems.
The operating and maintaining personnel of the biovac aspiration systems must have the
technical competence required to perform the work that has to be done.
The user must authorize the operating personnel to do the work that has to be done.
The personnel must have read and understood the complete Operating Manual before using
the biovac aspiration systems.
The Operating Manual must be kept at the place of use and be available to the personnel
when required.
1.3 Intended Use
The layout of the biovac aspiration systems must be appropriate for the conditions of use.
The user bears the sole responsibility for this.
The biovac aspiration systems may only be operated under the conditions stated
–in the "Technical Data" section,
–on the rating plate, and
–in the technical specification for the order concerned.
The biovac aspiration systems have an integrated, highly chemical-resistant diaphragm
pump. It is used in chemical and biological applications to extract non-explosive liquid
residues safely and precisely.
1.4 Use for an Unauthorized Purpose
It is forbidden to use the pump for applications deviating from the technical data stated on
the type plate or the conditions stated in the supply contract, or to operate it with missing or
defective protective devices.

Important Information
112037 5
1.5 Safety Devices
Measures such as the following are for the safety of the operating personnel:
operating mode S1 (with grounding connector)
integrated fuse in the vacuum pump
closed housing
intact collecting tank
insertion of a particle filter suitable for the work task
1.6 Meaning of the Warning notes
Take note of the warning notes. They are in the following box:
CAUTION / WARNING !
Hazard which may lead to serious injuries or material damage.
1.7 Product Standards, Safety Regulations
The biovac 106 Aspiration Systems fulfils the following product standards:
DIN EN ISO 12100:2011-03
Safety of machinery -
General principles for design - Risk assessment and risk reduction
DIN EN ISO 13857:2008-06
Safety of machinery - Safety distances to prevent hazard zones being reached
by upper and lower limbs
DIN EN 1012-2:2011-12
Compressors and vacuum pumps - Safety requirements -
Part 2: Vacuum pumps
DIN EN ISO 2151:2009-01
Acoustics - Noise test code for compressors and vacuum pumps - Engineering
method (grade 2)
DIN EN 60204-1:2014-10
Safety of machinery - Electrical equipment of machines -
Part 1: General requirements
DIN EN 61000-6-2:2011-06
DIN EN 61000-6-4:2011-09
Electromagnetic compatibility (EMC) -
Part 6-2: Generic standards - Immunity for industrial environments
Part 6-4: Generic standards - Emission standard for industrial environments
DIN EN 61010-1/A1:2015-04
Safety requirements for electrical equipment for measurement, control and
laboratory use - Part 1: General requirements
DIN EN 50110-1:2014-02
Operation of electrical installations
Directive 2012/19/EU
Electrical and electronics - old devices (WEEE)
Directive 2011/65/EUDangerous materials in electrical and electronics devices (RoHS II)
China - RoHS II Environment protection law - China 2016-01
The following additional safety regulations apply in the FR Germany:
BGV A3
Electrical equipment and operating materials
VBG 5
Power-driven machines
BGR 120
Guidelines for laboratories
BGI 798
Hazard assessment in the laboratory
BGG 919 (VBG 16)
Accident prevention regulations for "compressors"
BGR 189 (BGR 195;192;197)
Use of protective working clothes
Observe the standards and regulations applying in your country when you use the aspiration
systems.

Basic Safety Instructions
6 112037
2 Basic Safety Instructions
2.1 General information
WARNING !
Warning notices must be observed. Disregarding them may lead to damage to health
and property.
The biovac 106 Aspiration Systems must be operated by personnel who can detect im-
pending dangers and take action to prevent them from materialising.
The manufacturer or authorized workshops will only service or maintain the aspiration sys-
tems if it is accompanied by a fully completed damage report. Precise information about the
contamination (also negative information if necessary) and thorough cleaning of the system
are legally binding parts of the contract.
Contaminated aspiration systems and their individual parts must be disposed of in accor-
dance with the legal regulations.
The local regulations apply in foreign countries.
2.2 Electricity
The biovac 106 Aspiration Systems are supplied for operating mode S1. Please note that
the testing must be repeated in accordance with DIN EN 0105, DIN EN 0702 and BGV A2 in
case of portable devices.
The local regulations apply in foreign countries.
Please note the following when connecting to the electrical power supply system:
The electrical power supply system must have a protective connector according to DIN
VDE 0100-410 (IEC 60364-4-41).
The protective connector must not have any breaks.
The connecting cable must not be damaged.
2.3 Mechanical System
Improper use can lead to injuries or material damage. Observe the following instructions:
Only operate the biovac aspiration systems with hoses of the specified dimensions.
Solid particles in the pumping medium impair the pumping action and can lead to dam-
age. Prevent their penetrating into the pump.
Hazardous substances must be separated out as far as this is technically possible before
they reach the pump.
External mechanical stresses and vibrations must not be transmitted to the system. Only
use a flexible laboratory hose for connecting the aspiration system.
The overpressure generated at the pressure port must not exceed 1 bar.
The pump must not be used to pump liquids.
Set the biovac aspiration systems on a flat and horizontal surface.
Do not close the space beyond the bottom of the device in order to enable the pump to
cool.

Basic Safety Instructions
112037 7
2.4 Hazardous Substances
The responsibility for using the biovac aspiration systems rests with the operator.
Hazardous substances in the gases to be pumped can cause personal injuries and property
damage. Pay attention to the warning notices for handling hazardous substances.
The local regulations apply in foreign countries.
Explosive gases
The aspiration system is not certified according to ATEX guidelines 2014/34/EU.
The system operator is obliged to comply with the ATEX 137 guidelines 1999/92/EC when
us-ing the pump within and for danger areas.
Aggressive gases
An MP series diaphragm pump is used for extracting vapours and aggressive gases.
The warranty shall lapse if the biovac aspiration systems are used with diaphragm pumps
from other manufacturers.
Poisonous gases
Use a suitable separator when pumping poisonous or harmful gases. Prevent such sub-
stances from leaking out of the appliance or pump. Treat these substances according to the
applicable environmental protection regulations.
The diaphragm pump, control valves and hose lines can be damaged by poisonous or ag-
gressive gases.
Test the strength and leak-tightness of the connecting lines and the connected apparatus.
Prevent environmental poisons, e.g. mercury, getting into the diaphragm pumps.
Fulfil the requirements, for example:
German Hazardous Substances Regulation (GefStoffV) of 01. December 2010
Regulations 2016/1179/EU
(classification, packaging and identification of hazardous substances),
Manufacturer's safety data sheets on hazardous substances.
2.5 High Temperatures
The diaphragm pump may heat up as a result of the temperature of the gas being pumped
and through compression heat.
Prevent the following maximum permissible temperatures from being exceeded.
+ 40 °C for the environment and
+ 40 °C for the medium to be pumped.
The motor for single phase alternating current is protected against overload by a fine-wire
fuse and integrated motor-protective switch.

Description
8 112037
3 Description
3.1 Design
►Aspiration System biovac 106 with secretion glass container 2 liters
A filter holder for a PTFE filter is located between the secretion glass container (1) and the
diaphragm pump (2). Filters down to a minimum pore size of 0.22 µm may be inserted in this
holder. According to the filter fineness used, it is possible to achieve different types of filtra-
tion, enabling, among other uses, the handling of bacteria and viruses.
The cap (3) of the secretion glass container consists of a plastic cap with a seal.
Fig. 1a Aspiration-System biovac 106 with secretion glass container 2 liters
A quick coupling (4) is used for the connection to the diaphragm pump (2). It is provided with
a stop valve.
The used-resistant diaphragm pump (2) used has a long useful life.
Secretion container (1) and handvac (5) are connected with a hose (6). After disconnecting
the unions (7), the two flexible tube ends at the container may be connected to one another
to ensure safe transport.
The Aspiration System is switched on and off directly at the device switch or the optionally
available foot switch (9).
The user appropriate pipette tips (8) can be used in the respective adapter of the handvac
(5). All hoses (6) located outside of the Aspiration System are made of silicone.
(9) Option
(2)
(4)
(3)
(6)
(5)
(8)
(7)
(1)
(6)
(6)

Description
112037 9
►Aspiration System biovac 106 with secretion PP - container 4 liters
Between secretion - PP container (1) and membrane pump (2) is a inline filter (10) with a
pore size of 0.22 microns to protect the membrane pump against pollution caused by fine
solid particles and aerosols.
Fig. 1b Aspiration-System biovac 106 with secretion PP - container 4 liters
3.2 Function
The biovac Aspiration Systems with an integrated resistant diaphragm pump is used for the
safe and precise aspiration of non-flammable chemical and biological liquids.
The fluids can be removed easily and very precisely from slides, Petri dishes, cell culture
containers etc., by using different pipets or glass tips which are inserted into the handvac.
The integrated secretion container has a built-in float valve. This valve shuts the suction line
automatically as soon as the maximum fill level is reached.
A hydrophobic PTFE filter with a suitable filtration grade is inserted in order to provide
additional safety. The scope of supply includes a filter with a filtration grade of 1 µm.
(10)
(4)
(7)
(5)
(1)
(2)
(7)
(6)

Description
10 112037
3.3 Materials of the medium-affecting pump parts
Component
Materials
Seal
EPDM
Screw fitting / Connecting element
PVDF, PP
Valve
PEEK
Formed diaphragm
Elastomer + PTFE Layer
Vacuum hose
PTFE
Connection head / Pump head
PTFE with carbon-fibre reinforcing *)
*) electrically conductive (with manufacturer's certificate of electrical conductivity)
Material resistance to aggressive media see: Publisher Hoppenstedt Publishing (18. September 2007)
3.4 Areas of Application
The biovac 106 Aspiration Systems are intended for:
the safe and precise extraction and catching of liquid and non-explosive excess fluids
use in the chemical, biological and medical areas
generating a vacuum down to an ultimate pressure < 100 mbar
3.5 Possible Accessories
Designation
Order numbers
for biovac 106:
112037
112037-04
Seal for cover of secretion glass container
828840-4
-
PTFE filter 1 µm for cover of secretion glass container
828840-2
-
Inline filter 0.22 µm hydrophobic (10 pack)
112555-04
-
Foot switch
112529
Mains connection cable IEC with plug type12 (CH)
825877
3.6 Scope of Delivery
The scope of delivery is specified in the supply contract.

Technical Data
112037 11
4 Technical Data
4.1 Dimensions
Fig. 2 Dimension - biovac 106 with secretion glass container 2 liters
Fig. 3 Dimension - biovac 106 with secretion PP - container 4 liters

Technical Data
12 112037
4.2 Device Data
Parameter
Unit
biovac 106
with glass container 2 L
biovac 106
with PP-Container 4 L
Pumping speed (50/60 Hz)
DIN 28432 with speed of 1500 rpm
m3/h (l/min)
0.72 (12/16)
Ultimate pressure
mbar
100
Maximum inlet - / outlet pressure
bar
1
Intake connection
-
handvac (Pipettor)
Exhaust connection
Hose nozzle DN 8
for hose inside diameter 8 mm
Secretion glass container
-
2 liters
-
Secretion PP - container
-
4 liters
Ambient temperature
°C
+ 10 to + 40
Medium temperature
+ 40
Bearing
-
maintenance-free
Reference surface sound
pressure level DIN EN ISO 2151
dB (A)
45
Voltage
V
115 / 230
Frequency
Hz
50/60
Power
W
0.45
Fine fuse
A
F 3.15
Operating mode
-
S 1
Type of protection DIN EN 60529
IP 40
Class of insulation DIN EN 600034-1
F (160°C)
Dimensions (W/D/H) (without hose)
mm
342/363/197
395/363/197
Weight
kg
8.0
Order number:
-
biovac 106
inclusive mains connection cable IEC +
plug CEE, UK, US
112037
112037-04
4.3 Intake Pressure/Pumping Speed –Diagram
Fig. 4 Intake pressure pumping speed
The information presented in this material is based on technical data and test results of nominal units. It is believed
to be accurate and reliable and is offered as and aid to help in the selection of products.
It is the responsibility of the user to determine the suitability of the product for the intended use and the user as-
sumes all risk and liability whatsoever in connection therewith. Gardner Denver Thomas GmbH does not warrant,
guarantee or assume any obligation or liability in connection with this information.

Installation and Operation
112037 13
5 Installation and Operation
5.1 Unpacking
Carefully unpack the biovac 106 Aspiration System.
Check for:
Transport damage,
Conformity with the specifications of the supply contract (type, electrical supply data),
Completeness of the delivery.
Please inform us without delay if there are discrepancies between the delivery and the con-
tractually agreed scope of delivery, or if damage is detected.
Please take note of the general terms of business of the manufacturing firm.
In case of a claim under warranty, the device must be returned in packaging that is
suitable for protecting it during transport.
5.2 Installation and Connection
Procedure:
Fig. 5 Rear side - connections
(biovac 106
with secretion glass container 2 liters)
1.
Set the aspiration system on a flat and
horizontal surface.
2.
Connect the “handvac” to the suction line
(A). (see also in appendix operation manual)
3.
Connect the exhaust pipe to the
building ventilation system (B).
4.
If required, connect the foot switch
(accessories optional) to the socket (C)
provided on the unit.
5.
Set the mode selector switch (D) to
"Hand" or "Foot". (see chapter 3.5)
6.
Voltage selector 115/230 V (E)
Label on device:
Instructions examine and label remove!
7.
Connect the system to the power
supply (F).
8.
Switch on the unit's main switch (G).

Installation and Operation
14 112037
5.2.1 Connection schematic –biovac 106
handvac professional
Order no. 112580
Secretion glass container 2 Liters
complete
Order no. 112523-1
Basic unit biovac 106
Order no. 112573
Secretion PP - Container 4 Liters
complete
Order no. 112523-7
Basic unit biovac 106
Order no. 112573-02
a
handvac
for aspiration into
the container
c
Coupling plug
g
Elbow plug with valve
d
Separator
h
Connecting coupling
of the pump
e
Float valve
b
Coupling
f
PTFE Filter 1 µm (2 Liters container)
i
Diaphragm pump
Inline filter 0.22 µm (4 Liters container)
(hydrophobic)
-
-
b
Coupling
j
Exhaust connection
Hose nozzle DN 8
c
Coupling plug
Fig. 6 Connection schematic –biovac 106
5.3 Operation
CAUTION!
Observe the basic safety instructions when using the aspiration systems!
CAUTION!
Before the device is switched on, the voltage selector must be set with a screwdriver
to the voltage of the local power supply, either 115 or 220 V (+/-10%).

Installation and Operation
112037 15
Procedure:
1. The biovac aspiration systems is switched on and off at the operating switch (illuminated
rocker switch).
2. Set mode selector switch to "Hand".
3. For operation using the optional foot switch, set the selector switch to the "Foot" position
and actuate that switch.
4. A low air pressure is generated in the reservoir.
5. Press the black button at the top side of the “handvac” to suck the fluid into the reservoir.
6. A regulator screw is located at the bottom side of the “handvac”. It is used to set the ex-
traction speed.
7. For the safety of the user, a 55 mm PTFE filter (if necessary hydrophobic) suitable for
the requirements and work task must be inserted into the filter casing.
CAUTION !
Please observe the operating instructions included when using the "handvac" !
5.4 Storage
The pumps are to be stored in a low-dust, interior room within the temperature range from
+ 5 to + 40 °C and at a relative air humidity < 90%.
Leave the protective elements on the intake and pressure ports. Another equally good pro-
tection may be used.
5.5 Scrap Disposal
CAUTION !
The aspiration systems must be disposed of in accordance with the 2012/19/EU
guideline and the specific national regulations.
Contaminated systems must be decontaminated according to the laws.
The user is responsible for disposing of the products extracted and decontaminating the se-
cretion container and hoses.
Secretion glass container and container cover are autoclavable. Against hoses and pipettes
are expendable materials.
A contaminating of the diaphragm pump is to be avoided by use of a suitable filter.
The used materials of the gas-affecting parts are glass, PP, PEEK, PTFE and EPDM.

Maintenance and Servicing
16 112037
6 Maintenance and Servicing
6.1 General Requirements
Repairs of the biovac 106 Aspiration Systems may only be performed by the manufacturer
or authorized workshops. The prerequisites are a complete and factually correct damage re-
port, and a clean and, if necessary, a decontaminate device.
Send in defective devices for repair either to the manufacturer or to an authorized workshop.
The information about the contamination or thorough cleaning is legally binding parts of the
contract.
6.2 Maintenance Performed by the User
WARNING !
Only perform the work that is described here, and that which is permitted to be done
by the user.
All other maintenance and service work may only be performed by the manufacturer
or a dealer authorized by him.
Beware of the pump parts being possibly contaminated by hazardous substances.
Wear protective clothing if there is contamination.
The operator may perform maintenance work to the extent indicated below:
WARNING !
Before opening the pump unplug it from the mains.
6.2.1 Maintenance of the aspiration systems
6.2.1.1 Disassembly
Disconnect the power supply by pulling the device plug.
Disconnect the hose connections.
To empty, clean and decontaminate the secretion container, lift it up out of the holder of
the aspiration system.
Unscrew the suction connection and exhaust air filter.
Unscrew from below the four inner screws on the device.
Lift the hood off. Now, you can start with the maintenance of the diaphragm pump accord-
ing to chapter 6.2.2.
WARNING !
Wear protective gloves or protective clothing if necessary!
Do not clean with compressed air!

Maintenance and Servicing
112037 17
6.2.1.2 Assembly
Assembly takes place in reverse sequence. Use care when carrying out these activities,
and check for the proper fit of the couplings.
6.2.1.3 Test
Connect a vacuum measuring device to the intake port and check the ultimate pressure.
If the device is working properly, then the figure stated in the technical data must be attained
within a maximum of one minute.
6.2.2 Maintenance of the diaphragm pump
Scope of permissible work:
Inspect the pump chambers, diaphragms and valves,
Deposits in the inside of the pump must be cleaned out,
Change the diaphragms, valves and seals.
Tools required:
Tool kit: Order no. 402107, consists of:
Order no. 826801-4 Cross-head screwdriver, size 2,
Order no. 826801-2 Open spanner, size SW 14.
6.2.2.1 Disassembly
1. Disconnect the power supply and ensure that it cannot be switched on again.
2. To open the cover of the casing, remove the 4 screws from the unit's bottom side.
3. Open the screw clamps of the hose bridge on the pump body with the open spanner,
size 14.
4. Remove 2 x 4 screws (1) from each connecting head (2) with a cross-head screwdriver,
size 2.
5. Lift off the connecting head (2) and the pump head (5). The diaphragm is now freely
exposed.
6. Loosen the defective diaphragm (6) by turning it anticlockwise.
7. Valves (4) and o-rings (3) are located between the connecting and the pump head.
When dismounting both heads these parts are accessible.
8. Clean the valves (4), o-rings (3) and diaphragm (6) with a soft cloth and acetone and
replace defective items if necessary.
Fig. 8 Disassembly - Assembly

Maintenance and Servicing
18 112037
WARNING !
Renew defective parts, if necessary! Wear protective gloves!
Parts must be renewed at the intervals stated in this Operating Manual or as speci-
fied by the user internally!
Do not clean with compressed air!
6.2.2.2 Assembly (see Fig. 8)
1. Place the pump so that the diaphragm (6) is lying in a horizontal position.
2. Tighten the diaphragm (6) with the torque of 5 - 6 Nm.
3. Bring the connecting rod (see Fig. 10) and the diaphragm (6) into the central position.
4. Replace the pump head (5).
5. Insert the valves (4) and the o-rings (3). Ensure that they are lying completely flat.
Do not insert the burred side facing the sealing surface.
6. Replace the connecting head (2) and tighten the 2 x 4 cross head screws (1) with
a torque of 3 - 4 Nm.
7. Use an analogue assembly sequence for all heads.
8. Reattach the hose connections with clamping ring screw fittings.
9. Close the casing by shutting the cover.
6.2.2.3 Test
Connect the pump to the electrical supply.
Connect a vacuum measuring device to the suction connector and measure the ultimate
pressure.
If the device is working properly, then the figure stated in the technical data must be at-
tained within a maximum of one minute.
The pump must not make any abnormal noises.
Moving parts must not touch each other.
6.2.3 Maintenance of other components
Check that the glass components are undamaged cleaned and if necessary replace.
Empty the secretion glass container in a timely manner.
(Observe all disposal specifications as applicable to hazardous substances!)
Check screw connections for tightness and tightened when necessary.
Check vacuum hoses for leaks and, if necessary, replace them.
Check for leaks and, if necessary, replace the formed gasket located at the head piece of
the drip pan.
Change the PTFE filter and/or Inline filter at regular, defined intervals.
Test performance of the quick-fitting couplings with shut-off valves.

Maintenance and Servicing
112037 19
WARNING !
When repairing contaminated units, be sure to observe the applicable user specifica-
tions regarding decontamination as required.
Provide full information about the type of contamination and the used materials and
clean the pump thoroughly before handing it over to third parties.
6.3 Maintenance by the Manufacturer
Repairs and maintenance going beyond the extent of the work described in chapter 6.2 or
reconditioning or modification may only be performed by the manufacturer or authorized
workshops.
CAUTION !
The user shall be liable for the consequences of an incorrect damage report or a
contaminated pump. The statements in the damage report are legally binding.
6.4 Damage Report
You find the form of the damage report to the Download on our web page in the menu "ser-
vice" and "Downloads". www.welchvacuum.com
If you should not have an entrance to the Internet, you can request the form also gladly with
us, under phone +49 3677 604 0.
WARNING !
Incomplete or incorrectly completed damage reports may endanger the service per-
sonnel!
Give full information in the damage report, in particular regarding a possible con-
taminating.

Troubleshooting
20 112037
7 Troubleshooting
Only manufacturing firm and authorized service workshops may work in the biovac 106
Aspiration System and accessory components during the warranty period.
Trouble
Cause
Remedy
by:
with:
Vacuum pump
does not start
no power supply
Qualified
electrician
Check electrical installation
Motor defective
Service
workshop
Exchange
Pump body defective
Repair and/or exchange
Vacuum pump
does not
generate a
vacuum or
only an
inadequate
one
Connected apparatus
and/or
connecting elements
leaking
User or
Service
workshop
Identify and seal the leak,
replace the seals and/or
hoses if necessary.
Vacuum pump leaking
Check the hose
connections between the
pump heads, replace the
hoses and/or fittings if
necessary.
Pump head leaking
Service
workshop
Repair and/or exchange
Diaphragm defective
User or
Service
workshop
Exchange of the diaphragm
(see chapter 6.2)
Valve defective
Exchange of the valve
(see chapter 6.2)
Vacuum pump dirty
General maintenance /
leaning
Valves dirty
Cleaning condensates
and foreign objects out of
the valves.
Running noise
Vacuum pump dirty
User or
Service
workshop
General maintenance /
cleaning
Glass
components
defective
and/or leaking
User
Exchange of the glass parts
or seals
Cable(s)
defective
and/or brittle
Qualified
electrician
Exchange of the cable(s)
This manual suits for next models
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