K-Systems G210 InviCell User manual

Document K32903(12) | Date: March 25, 2020 | DRF: 5394
2797
User Manual
Models: InviCell Standard and InviCell Plus
with SignipHy™pH Monitoring System
G210 InviCell
CO2/O2 Incubator
Only

Contents
Section 1 - Preface 6
Section 2 - Safety 7
Safety and Reliability 7
Warnings 7
Cautions 8
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions 9
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity 9
Symbols 11
Section 3 - Installation 13
Before Installation 13
Placement 13
Section 4 - Device Description and Intended Use 14
Indications for Use 14
Applicable Part Numbers 14
Significant Performance Characteristics 14
Operation Principle 14
User Profile 14
Dish Inserts 15
Chamber Heating 15
Chamber Lid 15
Preparation Chamber 15
Section 5 - Product Overview 16
Main Components 16
Supplied Accessories for G210 InviCell Standard 17
Accessory Order Codes 18
Specification Table 19
Section 6 - G210 InviCell Plus with SignipHy™
pH Monitoring System 20
External Sensors, pH / CO220
Dish Insert for pH monitoring 21
External Temperature 21
Additionally Supplied Accessories for G210 InviCell Plus with SignipHy pH Monitoring System 21

Contents
Section 7 - Set-up 22
Gas Supply 22
Factory Settings 22
Section 8 - Basic Operation 23
Touchscreen Menu 23
Main Menu 24
Advanced Menu 24
Chamber Information 25
Edit Chamber Information 25
Log 26
Setpoint 26
Changing the Temperature Setpoint 27
Changing the Gas Setpoint 27
Section 9 - Settings 28
Changing the Date and Time 28
Ethernet Settings 29
Changing the Preparation Chamber Settings 29
Changing Language 29
Changing Basal Body Temperature 29
Security Settings 30
Access Levels 31
Edit User 32
Change Password 32
Create a New User 33
Delete User 33
Log Out 33
Lost Password 33
Alarm 34
External Alarm Connector 34
Errors 34

Contents
Section 10 - K-Link 35
Starting K-Link 35
Device Connection 35
Measurement Section 36
Alarm Display Section 36
Graph Section 37
Level Tab 37
Pressure Tab 38
Daily Average Tab 38
Warning Tab 39
Mail Tab 39
Service Tab 40
Section 11 - Troubleshooting 41
Heating System 41
CO2Gas Regulator 41
O2Gas Regulator 41
Gas Consumption 42
Touchscreen 42
Section 12 - Maintenance 43
Preparation at the Point of Use 43
Periodic Cleaning 43
Disinfection 43
Drying 43
Sterilizing the Dish Inserts 44
Validation Check 44
Gas Sample Port 45
Chamber Lid Plug 46
Verification of Gas Concentration in Chambers 46
Temperature Calibration 47
Section 13 - Service 48
Service plan 48
On-screen Prompts 48
Replacing the Origio Gas line Filter 49
Disposal of the Origio Gas line Filter 49

Preface
1
5
Section 14 - Disposal and Recycling 50
Environmental Protection for Disposal of the Product 50
Recyclable Components 50
Section 15 - Warranty Information and Limits
on Liability 51
Section 16 - Returning Product to CSI for Repair 52
Customer Service Contact Details: 53
US Only Customers Contact Details: 53

Preface
1
6
Section 1 - Preface
Thank you for choosing a K-Systems product.
At CooperSurgical, we strive to provide the very best products and solutions for human IVF and the
G210 InviCell is designed to provide optimum conditions for gametes and embryos during long-term
culture.
For optimal use of the G210 InviCell, please read and follow the instructions in this User Manual.
The incubator should be operated by trained personnel only. All sections of this manual should be
read and understood fully before any operation of the incubator. If the operator is unsure of any of
the information contained in this manual they should contact Customer Services or an appointed
representative before attempting to use this equipment. Keep these instructions close to the device.
This ensures easy access to the safety instructions and important information.
In no event does CooperSurgical assume the liability for any technical or editorial errors of commission,
or omission; nor is liable for direct, indirect, incidental, or consequential damages arising out of the
use or inability to use this manual.
The information in this manual is current at the time of publication. Our commitment to
product improvement requires that we reserve the right to change equipment, procedures
and specifications at any time. The latest version of the User Manual can be downloaded from
origio.com. This user manual belongs with the G210 InviCell incubator and should be passed on with
the incubator if relocated to another facility.
© This manual is protected by copyright, all rights reserved, and no part hereof may be photocopied
or reproduced in any form without the prior written consent of CooperSurgical.
95 Corporate Drive
Trumbull
CT 06611
USA
EMERGO EUROPE
Prinsessegracht 20
2514 AP The Hague
The Netherlands
OCTAX Log & Guard™is a trademark of Vitrolife AB
TrakStation®is a registered trademark of Blood Cell Storage, Inc
SignipHy™is a trademark of CooperSurgical, Inc.
Oosafe®is a registered trademark of Sparmed a/s.
CooperSurgical®is a registered trademark of CooperSurgical, Inc.
K-Systems is a CooperSurgical brand.
©2019 CooperSurgical, Inc.

Safety
7
2
Section 2 - Safety
Safety and Reliability
Please read this manual carefully and follow the instructions to ensure that the system will work safely
and reliably. Safety is the responsibility of the laboratory. Risk assessment and working practices
should comply with local regulatory policies.
Warnings
WARNING: Use only 100% pure CO2and 100% pure N2gas. Use of other gases could
result in serious injury, depending on the gas connected.
DO NOT disassemble or modify any part of the G210 Invicell, or substitute any
component for any other. Doing so may result in damage to samples. This voids the
warranty and/or service contract.
WARNING To avoid the risk of electric shock, this equipment must only be connected
to a mains supply with protective earth.
WARNING Not to be used in a patient environment.
WARNING Use of accessories, transducers and cables other than those specified
or provided by the manufacturer of this equipment could result in increased
electromagnetic emissions or decreased electromagnetic immunity of this equipment
and result in improper operation.

Safety
8
2
CAUTION
• Caution: Federal law restricts this device to sale by or on the order of a physician or a
practitioner trained in its use.
• DO NOT use the incubator if ShockWatch or TipNTell has been triggered or if the package
is damaged.
• Read and understand the manual completely before use. Keep the manual close to
the unit.
• Never use or handle this unit in ways other than specified in this manual. The user’s safety
may be at risk and the unit may get damaged.
• Never try to move the unit without consulting a person authorized by CooperSurgical.
• Never use the unit if the alarm system of the device has issued a failure message and the
cause of the failure has not been identified.
• Protect the power cord from being damaged or being restricted in any way. Unplug the
power cord from the wall socket or at the rear of the instrument to disconnect the mains
supply.
• Make sure that CO2and N2gas supply pressures are maximum 1.0 bar and not below 0.5
bar.
• Always keep the red cap on unused gas inlets at the back of the unit and the protection cap
on the sample port placed behind the Preparation Chamber.
• Never use the unit without a genuine Origio Gas Line Filter.
• DO NOT expose the filter to liquids. Change filters that have been exposed to liquids.
• DO NOT leave lids open for more than 20 seconds.
• DO NOT use the unit at ambient temperatures exceeding 30°C. Ambient temperature
above 30°C will compromise the incubation process. The relative humidity must not exceed
75% (non-condensing).
Cautions

Safety
9
2
The G210 is intended for use in the electromagnetic environment specified below. The customer or the user of
the G210 should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR11 Group 1
The G210 uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions
CISPR11 Class A – Complies The G210 is suitable for use in all establishments other than domestic and those directly connected to the public low-
voltage power supply network that supplies buildings used
for domestic purposes.
Harmonic emissions
IEC 61000-3-2 Class A - Complies
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Class A - Complies
Guidance and Manufacturer’s Declaration – Electromagnetic
Immunity
The G210 is intended for use in the electromagnetic environment specified below. The customer or the user of
the G210 should assure that it is used in such an environment.
IMMUNITY Test IEC 61326-1
Test level Compliance level Electromagnetic environment - guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
+ 4 kV contact
+ 2, 4, 8 kV air
+ 2, 4 kV contact
+ 2, 4, 8 kV air
Floors should be wood,
concrete or ceramic tile.
If floors are covered with
synthetic material, the relative
humidity should be at least
30 %.
Electrical fast transient/
burst
IEC 61000-4-4
+/- 1.0kV Burst Potential -
Mains
+/- 0.5kV Burst Potential -
Signals/Control
+/- 1.0kV Burst
Potential - Mains
+/- 0.5kV Burst
Potential - Signals/
Control
Surge
IEC 61000-4-5
Line-Line: 0.5kV
Combination Wave (1.2μS
x 50μS Voltage, 8μS x 20μS
Current)
Line-Earth: 0.5kV & 1.0 kV
Combination Wave (1.2μS
x 50μS Voltage, 8μS x 20μS
Current)
Line-Line: 0.5kV
Combination Wave
(1.2μS x 50μS Voltage,
8μS x 20μS Current)
Line-Earth: 0.5kV & 1.0
kV Combination Wave
(1.2μS x 50μS Voltage,
8μS x 20μS Current)
Voltage dips, short
interruptions and voltage
variations on power
supply input lines
IEC 61000-4-11
100% Reduction; 0.5-1
50Hz Period Cycles; 0° &
180° Sync Angle
30% Reduction; 0.5s
Duration; 25 50Hz Period
Cycles; 0° & 180° Sync
Angle
100% Reduction; 5s
Duration; 250 50Hz Period
Cycles; 0° Sync Angle
100% Reduction; 0.5-1
50Hz Period Cycles; 0°
& 180° Sync Angle
30% Reduction; 0.5s
Duration; 25 50Hz
Period Cycles; 0° &
180° Sync Angle
100% Reduction; 5s
Duration; 250 50Hz
Period Cycles; 0° Sync
Angle
Guidance and Manufacturer’s Declaration – Electromagnetic
Emissions

Safety
10
2
IMMUNITY Test IEC 61326-1
Test level
Compliance
level
Electromagnetic environment -
guidance
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields should be
at levels characteristic of a typical commercial
environment.
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3Vrms, 0.150-80Hz, 80%
AM Modulation, 1s Dwell
Time
3 V/m
80 MHz to 1000 MHz
3V/m
1400 MHz to 2000 MHz
1V/m
2000 MHz to 2700 MHz
3Vrms, 0.150-
80Hz, 80% AM
Modulation, 1s
Dwell Time
3 V/m
3V/m
1V/m
Portable and mobile RF communications
equipment should be used no closer to any
part of the G210, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency
of the transmitter
Recommended separation distance
d = [ 3,5 ] √P
3
d = [ 3,5 ] √P 80 MHz to 800 MHz
3
d = [ 7 ] √P 800 MHz to 2,5 GHz
3
Where P is the maximum output power rating
of the transmitter in watts (W) according to
the transmitter manufacturer and d is the
recommended separation distance in metres
(m).
Field strengths from fixed RF transmitters,
as determined by an electromagnetic site
survey,a should be less than the compliance
level in each frequency range. b
Interference may occur in the vicinity of
equipment marked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site
survey should be considered. If the measured field strength in the location in which the G210 is used exceeds
the applicable RF compliance level above, the G210 should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating the G210.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

Safety
11
2
Symbols
Symbol Meaning
WARNING: Indicates a potentially hazardous situation which, if not
avoided, could result in death or serious injury.
CAUTION: Indicates a potentially hazardous situation which, if not
avoided, may result in minor or moderate injury. It may also be used
to alert against unsafe practices.
Consult the User Manual for information needed for proper use of
the device.
Manufacturer
Date of manufacture
Waste electrical and electronic equipment
• CooperSurgical, and its distributors within the European Union
and associated states, have taken the necessary steps to comply
with the directive 2012/19/EU on waste electrical and electronic
equipment (WEEE).
• The instrument, when reaching its end of life, must be collected
and recycled separately from other waste according to national
requirements. Please contact a local CooperSurgical distributor
for instructions.
Environmental implications: WEEE contains materials that are
potentially hazardous to the environment and to human health (see
page 50).
S
S
N
N
Serial Number
REF
REF
Catalog Number
In accordance with Annex II of the European Medical Device Directive
93/42/EEC, as amended by Directive 2007/47/EC.
2797
Glossary ISO 15223-1:2016

Safety
12
2
Symbol Meaning
This equipment must be protectively earthed
Only
Caution: US Federal law restricts this device for sale to or on the order
of a licensed healthcare practitioner.
Warranty label
Ethernet
Sample Port Sample port
GAS (MAX 1 BAR) Gas Inlets CO2/N2
Static sensitive (ESD)
Fuse
EC REP Authorized Representative in the European Community
Humidity limitation for storage and use
Non-condensing
Temperature limit for storage and use
Max 1 week at 50°C
95%
5%
50°C
-5°C

Installation
13
3
Section 3 - Installation
Installation of the G210 InviCell should be carried out by a CooperSurgical Service Technician or other
authorized personnel. Incorrect installation could result in overall poor performance.
The G210 InviCell is designed as a stationary unit and, therefore, not to be moved once it has been
installed. If the incubator needs to be relocated, please contact Customer Service.
Before Installation
This incubator is transported in a crate and inspection after delivery is recommended. If the ShockWatch
or TipNTell has been triggered, inform Customer Service.
Check the contents to ensure all parts listed on the packing list are present.
Placement
The G210 InviCell should be placed on a level, secure surface, away from heaters, coolers,
air-conditioning outlets, mists, splash and direct sunlight. Allow 10cm of clearance on all sides to allow
adequate ventilation.
Allow the G210 to acclimatize for two hours before installation.
To maintain a device setpoint between 35-40°C the preferred ambient temperature should be
between 20-30°C. DO NOT use the incubator at ambient temperatures exceeding 30°C as this may
compromise the incubation process.
This unit is designed for use at altitudes under 2,000 meters.
HANDLE WITH CARE
WARNING
RED INDICATES ROUGH HANDLING.
IF RED, NOTE ON THE BILL OF LADING
AND INSPECT PRODUCT
PRODUCT OF MEDIA RECOVERY
MODEL: L-65 (25g)
MADE IN THE USA
www.shockwatch.com 1.800.527.9497
MADE IN THE U.S.A
BLUE BEADS IN
ARROW INDICATES
CONTAINER WAS
TIPPED OR
MISHANDLED
TELL
TIP
CAUTION
• Installation of the unit should only be performed by an authorized CooperSurgical Service
Technician.
• Never block any of the ventilation holes on the unit.
• Make sure that all devices emitting electromagnetic radiation are kept at a reasonable distance
from the unit in order to avoid any potential interferences.
• Make sure the power circuits used are intended for medical equipment.
• Make sure there is sufficient access to the device for ease of disconnection if required.

Device Description and Intended Use
14
4
Section 4 - Device Description and Intended Use
The G210 InviCell is a bench-top long-term incubator comprised of ten independent chambers for
gamete/embryo development and one larger preparation chamber. The larger preparation chamber
is not used for embryo development. The device is a non-sterile, reusable piece of equipment.
The incubator is used to culture gametes and embryos for up to 6-7 days in a controlled environment
(temperature, CO2/O2), normally in culture media contained within a culture dish. The CO2and O2
concentration are monitored by sensors located in a chamber internal to the incubator chassis. The
gas is constantly recirculated from the culture chambers through a HEPA (high-efficiency particulate
air) / VOC (volatile organic compound) filter.
The G210 InviCell Plus with SignipHy™ pH Monitoring System includes an accessory that monitors pH
by surrogate media samples using a fluorescent marker contained in a disposable sample cup. When
this cup is properly placed in the sensor fixture, the cup does not come in direct contact with the
culture dish or gamete/embryo. This disposable cup is supplied sterile and is single use.
The G210 InviCell overall dimensions are 860mm wide x 550mm deep x 180mm high, with a weight
of 53kg (maximum).
Indications for Use
The G210 InviCell Plus with SignipHy™ pH Monitoring System is a bench-top incubator that is intended
to provide a controlled environment at or near body temperature and gas levels (CO2, O2, and N2) for
the development of gametes and/or embryos during In Vitro Fertilization (IVF) / Assisted Reproductive
Technology (ART) treatments.
The G210 InviCell Plus with SignipHy™ pH Monitoring System includes an accessory for pH monitoring
of surrogate samples of bicarbonate-based culture media used for ART procedures.
Applicable Part Numbers
Order Code Description
K59500 G210 InviCell Standard
K60000 G210 InviCell Plus with SignipHy™ pH Monitoring System
Significant Performance Characteristics
The incubator has been developed and optimized for gametes and embryos cultured with an overlay
of either paraffin or mineral oil. Each chamber is designed to contain dishes from one patient only.
Operation Principle
The fertilized egg (zygote) is cultured for up to 6-7 days in a growth medium in the incubator with
a controlled environment (temperature and CO2/O2). It is then implanted in the same or another
woman’s uterus, with the intention of establishing a successful pregnancy.
User Profile
A trained health professional, who has the appropriate assisted reproduction technologies
qualifications. Only qualified personnel trained in using the G210 InviCell should operate the incubator.

Device Description and Intended Use
15
4
Operating Environment
To be used at ambient temperature in a medical environment, clinic or hospital laboratory under
normal working conditions.
Dish Inserts
The chambers should only be fitted with special Dish Inserts (1), that allow safe placement of standard
culture dishes (LifeGlobal, Falcon, Nunc, Vitrolife).
Ensure the culture dishes
are placed securely in the
correct milled grooves of
the Dish Inserts.
1
23
Chamber Heating
Each chamber is heated with K-Systems’ unique non-inductive EM Neutra™ heating system, which
provides a uniform heat distribution. All chambers are equipped with individual temperature sensors
to ensure stable temperatures at all times, and unidirectional gas flow across the chambers ensures
even gas distribution in each chamber.
Chamber Lid
Each lid has a sensor that, when opened, will disconnect the gas flow to minimize ambient air entering
the gas system. The gas flow restarts immediately after closing the lid.
The silicone plugs (2) in the lid of each chamber are for the collection of gas samples. These plugs
should be replaced when penetrated a maximum of 5 times.
Preparation Chamber
The Preparation Chamber (3) is intended to be used for the equilibration and heating of pre-filled
culture dishes with an oil overlay or flask of oil.
The Preparation Chamber also has a lid sensor which will disconnect the gas flow when the lid is
opened, to minimize the ingress of ambient air into the gas system. The gas flow restarts immediately
after closing the lid.
Gas flow to the Preparation Chamber can be disconnected through the user interface (see page 29).
CAUTION: If the equipment is used in a manner not specified by this manual, the
safety of the user may be at risk and the equipment may be damaged. Always use the
equipment as stated in this User Manual.

16
5
Product Overview
Section 5 - Product Overview
Main Components
Components
1 Incubator Chambers
2 Touchscreen
3 Preparation Chamber
4 Origio Gas Line Filter
4
2
3
1
G210 InviCell Standard and Plus models - front view
G210 InviCell Standard and Plus models - raised top section

17
5
Product Overview
5
7
On base
of unit
6
89 10
Supplied Accessories for G210 InviCell Standard
• 1 x Origio Gas Line Filter
• 2 x HEPA Inline Filter for input gas supply
• 10 Dish Inserts for LifeGlobal, Nunc®, Falcon®or Vitrolife®Customers to specify number and type when
ordering (minimum ordering quantity of 10)
• 2 x Silicone Tube Sealing Rings & Silicone Tube (3m)
• Gas sampling coupling
• 1 power cord
• 1 LAN cable (3m)
• 1 packet of Chamber Lid plugs (10 pieces)
• 1 USB drive containing K-Link software
Components
5 Product label
6 Mains connection with fuse
7 Ventilation holes
8 Gas inlet connectors
9 Alarm output
10 Ethernet connector**
**External computing devices connected to the Ethernet on the unit must only be Limited Power
Source and SELV circuit according to the standards IEC/UL 60950-1.
G210 InviCell Standard Model - back view
(see page 20 for InviCell Plus)

18
5
Product Overview
Accessory Order Codes
Order Code Description
23063-1 Falcon Dish Inserts 1 pc
23064-1 Nunc Dish Inserts 1 pc
23069 Vitrolife Dish Inserts 1 pc
23070 LifeGlobal Dish Inserts 1 pc
23080 Dish Inserts LifeGlobal pH (Plus models only)
23060-1 Dish Insert Nunc pH (Plus models only)
23061-1 Dish Insert Falcon pH (Plus models only)
23079 Dish Insert Vitrolife pH (Plus models only)
ULTRA 001 Origio Gas Line Filter
53830 HEPA Inline Filter
59922 Lid Plugs, bag of 10
59901-1 Lid Seal for culture chambers
59902-1 Lid Seal for Preparation Chamber
59688 Gas sampler coupling
11103 G100 Gas Analyzer
11006 Solid Temperature Sensor (use with K-Systems F100 Thermometer)
59655 XLR6 Receptacle Connector
32903 G210 User Manual
60017 Connector for External CO2sensor MTG (Plus models only)
60014 Connector for External CO2sensor Vaisala (Plus models only)
60018 25 Pin D-Sub male connector prepared for soldering (Plus models
only)
60019 24VDC power supply (Plus models only)
120040 SignipHy User Manual
SS-600019 SignipHy TrakStation®
SS-400019 SignipHy sv2 sensor
SS-400020 SignipHy qc2 alignment tool

19
5
Product Overview
Specification Table
Criteria Specification
Overall dimensions, (L x W x H) 860mm x 550mm x 180mm
Weight 53kg maximum
Temperature range 35 – 42°C
User interface Touchscreen
User interface functions Digital temperature readout, data logger, temperature
setpoint, calibration, warning for next service
Connections Mains, CO2gas, N2gas, Sampler port, Ethernet, Alarm
Alarms Visual and audible alarm for out of range temperature and gas
Filter (HEPA/ VOC) Origio Gas Line Filter
IP class IP30
Overvoltage category Transient overvoltage II
Pollution degree rating for electrical
equipment 2
Power specifications 100 – 240 VAC
Max consumption 270W
Voltage L/N/PE AC, 100 - 240VAC Class 1 type B
Frequency 50/60 Hz
Current 3A
Mains supply voltage fluctuations Up to +/-10 % of the nominal voltage
Fuses 100 - 250V UL Listed
Mains connection T4.0AL
Ambient conditions
Working temperature and humidity 20 – 30°C. Less than 75% RH (non-condensing)
Transport and storage temperature
and humidity
-5 – 50°C. Less than 95% RH (non-condensing)
Maximum one week at 50°C

20
6
G210 InviCell Plus
Section 6 - G210 InviCell Plus with SignipHy™
pH Monitoring System
G210 InviCell Plus with SignipHy pH Monitoring System supports external and independent monitoring
of parameters regarding the performance of culture media, CO2concentration, temperature and pH
measurement.
All external sensors are completely independent of the functions and controls in the G210 InviCell
Plus with SignipHy pH monitoring as they are connected to and powered by instruments independent
of the G210 InviCell Plus with SignipHy pH Monitoring System.
CAUTION: Installations of external sensors must be performed by CooperSurgical or
by persons authorized by CooperSurgical only.
Component
1 Connection for external CO2sensor
2 Connection for external pH monitoring (SignipHy™)
3 Data connection for external thermometer and power
4 Power connection for external thermometer and power
External Sensors, pH / CO2
The following external sensors can be used with the G210 InviCell Plus:
• External pH: SignipHy™ TrakStation®
• External CO2: OCTAX Log & Guard™ CO2sensor from MTG
GMP251 Carbon Dioxide Probe from Vaisala Oyj
The CO2sensor needs to be purchased separately, directly from MTG GMbH or Vaisala Oyj.
An external CO2connector for the GMP251 Carbon Dioxide Probe from Vaisala Oyj is enclosed.
Connectors can to be ordered separately.
• OCTAX Log & Guard™ CO2sensor from MTG
• GMP251 Carbon Dioxide Probe from Vaisala Oyj
1
234
G210 InviCell Plus - back view