Osstell ISQ Si-SQ User manual

module
Si-SQ
Instructions for Use
Edition USA

2
Contents
Symbols.......................................................................................................................................................................................................... 3
1. Introduction .............................................................................................................................................................................................. 6
2. Electromagnetic compatibility (EMC)..................................................................................................................................................... 8
3. Scope of delivery ...................................................................................................................................................................................... 9
4. Safety notes ............................................................................................................................................................................................ 10
5. Description............................................................................................................................................................................................... 11
6. Start-up .....................................................................................................................................................................................................12
7. Operation ...................................................................................................................................................................................................13
8. Hygiene and maintenance...................................................................................................................................................................... 16
9. Servicing .................................................................................................................................................................................................. 27
10. W&H accessories and spare parts....................................................................................................................................................... 29
11. Technical data ....................................................................................................................................................................................... 30
12. Disposal ................................................................................................................................................................................................. 32
Explanation of warranty terms................................................................................................................................................................... 34
Authorized W&H service partners.............................................................................................................................................................. 35
Manufacturer’s declaration......................................................................................................................................................................... 36

3
WARNING!
(if persons could be injured)
ATTENTION!
(if property could be damaged)
General explanations,
without risk to persons or property
Call customer serviceSterilizable
up to the stated temperature
Symbols in the Instructions for Use

4
Date of manufacture
Catalogue number
Serial number
Type B applied part (not suitable
for intracardiac application)
Do not dispose of with
domestic waste
Data Matrix code
for product information
including UDI (Unique Device
Identification)
CE mark
with identification number
of the Notified Body
XXXX
Symbols on the Osstell ISQ module
DC – direct current
Follow Instructions for Use

5
This way up
Caution! According to Federal law, this medical
device may only be sold by or on the order of a
dentist, physician or any other medical practitioner
licensed by the law of the State in which he or she
practices and intends to use or order the use of this
medical device.
Fragile, handle with care
Keep dry
Permitted temperature range
Humidity,
Limitation
»Der Grüne Punkt« (The Green Dot)
trademark of Duales System
Deutschland GmbH
Trademark of RESY OfW GmbH
for identification of recyclable
transport and outer packaging
of paper and cardboard
-40 °C (-40°F) Min.
+70 °C (+158°F) Max.
8 %
80 %
CE mark
with identification number
of the Notified Body
XXXX
Data structure in accordance with
Health Industry Bar Code
Data Matrix code
for product information
including UDI (Unique
Device
Identification)
Symbols on the packaging

6
1. Introduction
For your safety and the safety of your patients
These Instructions for Use explain how to use your product. However, we must also warn against possible hazardous situations.
Your safety, the safety of your team and, of course, the safety of your patients, are of paramount importance to us.
Observe the safety notes.
Intended use
Osstell ISQ is indicated for use in measuring the stability of implants in the oral cavity and craniofacial region Osstell ISQ can add
important information to the evaluation of implant stability and can be used as part of an overall treatment evaluation program. The
final implant treatment decisions are the responsibility of the user.
Misuse may damage the Osstell ISQ module and hence cause risks and hazards for patients, users and third parties.
Qualifications of the user
We have based our development and design of the Osstell unit for Implantmed on the “physician” target group.

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Introduction
Production according to EU Directive
The medical device complies with the regulations of Directive 93/42/EEC.
Responsibility of the manufacturer
The manufacturer can only accept responsibility for the safety, reliability and performance of the Osstell ISQ module
when compliance with the following instructions is ensured:
> The Osstell ISQ module must be used in accordance with these Instructions for Use.
> The Osstell ISQ module has no components that can be repaired by the user. Assembly, modifications or repairs
must only be undertaken by an authorized W&H service partner (see page 35).
> Unauthorized opening of the equipment invalidates all claims under warranty and any other claims.
In addition to unauthorized assembly, installation, modification of or repairs to the Osstell ISQ module and measuring probe
with cable, transmission instrument and non-compliance with our instructions, improper use will invalidate all claims made under
warranty or otherwise.

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2. Electromagnetic compatibility (EMC)
Medical electrical equipment is subject to particular precautions in regard to EMC and must be installed and put into
operation in accordance with the EMC notes included.
W&H guarantees the compliance of the device with the EMC requirements only when used with original W&H accessories
and spare parts. The use of accessories and spare parts not approved by W&H can lead to an increased emission of
electromagnetic interference or to a reduced resistance against electromagnetic interference.
HF communication equipment
Portable HF communications equipment (including peripherals such as antenna cables and external antennas) should be
used no closer than 30 cm (12 inches) to the medical device. Otherwise, degradation of the performance of this medical
device could result.
The medical device may be interfered by other equipment, even if these other devices comply with CISPR (International
special committee on radio interference) emission requirements.
Use of this medical device adjacent to or stacked with other equipment should be avoided because it could result in
improper operation. If such use is necessary, this medical device and the other equipment should be observed to verify that
they are operating normally.
The medical device is not intended for use in the vicinity of HF surgical devices.

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3. Scope of delivery
REF Description
30210000 Osstell ISQ module
07849900 TestPeg
0772180 0 Universal support
07460300 SmartPeg mount

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4. Safety notes General
> Before using the Osstell ISQ module for the first time, store it at room temperature for 24 hours.
> Check the Osstell ISQ module and the measuring probe with cable for damage and loose parts every time before use.
> Do not operate the Osstell ISQ module and the measuring probe with cable if it is damaged.
> Perform a test measurement with the TestPeg prior to every use.
> The responsibility for the use and timely shutdown of the system lies with the user.
> Ensure that it is possible to complete the operation safely should the units or instruments fail.
> The Osstell ISQ module is not approved for operation in potentially explosive atmospheres.
Do not twist or kink the cable! Do not coil it too tightly!
The Osstell ISQ module is classed as “conventional equipment” (closed equipment without protection against the ingress
of water).
Hygiene and maintenance prior to initial use
> Clean and disinfect the Osstell ISQ module and the measuring probe with cable.
> Sterilize the measuring probe with cable.

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5. Description
TestPeg
Osstell ISQ module
Measuring probe connection
USB cable Measuring probe with cable
SmartPeg mount

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Push in the Osstell ISQ
module until it locks audibly.
Pay attention to
the positioning
of the USB cable!
Connect USB.
Connect measuring probe.
Pay attention to
the positioning!
6. Start-up General

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7. Operation
> The TestPeg is for testing only and for teaching in the function.
> You can purchase SmartPegs from smartpegs.wh.com or osstell.com.
> SmartPegs are for single use only.
> SmartPegs are available for a range of different implant systems and can be used in combination
with all conventionally available implants.*
> Ensure that the sterile chain is not broken.
> Only use SmartPegs with intact packaging.
Select ISQ program.
The ISQ program always appears after the last program.
Pull a thread through the SmartPeg mount.
Tie the thread to your wrist to prevent loss.
Insert the SmartPeg into the SmartPeg mount.
The SmartPeg is magnetic and is held in place by SmartPeg mount. Check that it is retained secure hold.
Attach the SmartPeg to the implant or abutment by screwing the SmartPeg mount using finger force of
approximately 4-6 Ncm.
Do not overtighten the SmartPeg or the SmartPeg thread may be damage
* For further information, please contact an authorized W&H service partner or visit osstell.com

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Operation
Press the foot control pedal once to start the measurement.
Press the foot control pedal again to stop the measurement early.
Hold the measuring probe about 3 to 5 mm from the tip of the SmartPeg until the
measured value is displayed.
Measure in both the mesiodistal direction (a) and the buccolingual direction (b).
Do not measure from above.
Repeat 5 and 6 to perform multiple measurements.
The measured value is underlined in colour and confirmed by a signal tone.
Remove the SmartPeg with the SmartPeg mount.
b
a

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Measurement result*
The measurement result can be used as part of a general assessment program. The user bears the ultimate responsibility
for the decision for implant treatment.
This is a summary of scientific data and therefore does not represent an official recommendation.
To monitor osseointegration, measurements should be taken after implant insertion and before restoration of the implant.
Scientific studies can be found here www.osstell.com
ISQ value
The resonance frequency as a measure of implant stability is calculated from the oscillation frequency of the SmartPeg.
The results of this calculation are displayed as the ISQ value. The scale from the ISQ value ranges from 1 to 100.
* For further information, please contact an authorized W&H service partner or visit osstell.com
Operation
Low Stability Medium Stability High Stability
60 70
Red
ISQ <60
Implant at risk –
monitor ISQ
Yellow
ISQ 60 – 65
Full splint (immediate
loading)
2-stage
Traditional loading
Yellow
ISQ 65 – 70
Partial case
1- or 2-stage
Early loading
Green
ISQ >70
Single case
1-stage
Immediate loading
65
Indication
Surgical protocol
Restorative protocol

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8. Hygiene and maintenance
Follow your local and national laws, directives, standards and guidelines for cleaning, disinfection
and sterilization.
> Wear protective clothing, safety glasses, face mask and gloves.
> Use only oil-free, filtered compressed air with a maximum operating pressure of 3 bar for manual drying.
Cleaning agents and disinfectants
> Read the notes, follow the instructions and heed the warnings provided by the manufacturers of cleaning agents and/
or disinfectants.
> Use only detergents which are intended for cleaning and/or disinfecting medical devices made of metal and plastic.
> It is imperative to comply with the concentrations and exposure times specified by the manufacturer of the
disinfectant.
> Use disinfectants which have been tested and found effective by the Verbund für Angewandte Hygiene e.V.
(VAH = Association for Applied Hygiene), the Österreichischen Gesellschaft für Hygiene, Mikrobiologie und
Präventivmedizin (ÖGHMP = Austrian Society for Hygiene, Microbiology and Preventive Medicine), the Food and Drug
Administration (FDA) and the U.S. Environmental Protection Agency (EPA).
> The user is responsible for validating its process if the specified cleaning agents and disinfectants are not available.
General notes

17
Hygiene and maintenance
The product lifetime and the medical device’s ability to operate correctly are mainly determined by
mechanical stress during use and chemical influences due to processing.
> Send worn or damaged medical devices and/or medical devices with material changes to an authorized W&H service
partner.
Processing cycles
> We recommend a regular service for the measuring probe with cable after 250 processing cycles or one year.
> We recommend a regular service for the W&H universal support after 250 processing cycles.
Limitations on processing

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Hygiene and maintenance Initial treatment at the point of use
Wipe the Osstell ISQ module, the measuring probe with cable and the universal support and the irrigant support with
disinfectant.
Note that the disinfectant used during pre-treatment is only for personal protection and cannot replace the disinfectant
step after cleaning.

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Hygiene and maintenance Manual cleaning
Measuring probe with cable / Universal support
Do not immerse the measuring probe with cable and the universal support in liquid disinfectant or in an ultrasonic bath.
Measuring probe with cable / Universal support
> Clean the measuring probe with cable and the universal support under running tap water (< 35°C / < 95°F).
> Rinse and brush off all internal and external surfaces.
> Remove liquid residues using compressed air.
Osstell ISQ module
> Do not immerse the Osstell ISQ module in water or clean under running water.

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Hygiene and maintenance Manual disinfection
Measuring probe with cable / Universal support
> W&H recommends wipe-down disinfection.
Evidence of the basic suitability measuring probe with cable and the universal support for effective manual disinfection
was provided by an independent test laboratory using the »mikrozid® AF wipes« disinfectant (Schülke & Mayr GmbH,
Norderstedt).
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