implantmed SI-1010, SI1015, SI-1023 Instructions for Use Rev. 006 Jan 2021

Contents Symbols... 4 1. Introduction... 8 2. Electromagnetic compatibility (EMC)... 10 3. Unpacking... 11 4. Scope of delivery...12 5. Safety notes...13 6. Description... 20 of front panel... 20 of rear panel...21 of foot control S-N2/S-NW... 22 of motor with cable... 24 7. Start-up... 25 8. Control unit... 26 9. Starting operation... 27 10. Control unit operation... 28 Main menu... 28 Menue Navigation... 31 Factory settings... 36 Documentation with USB stick... 42 ioDent® platform... 44 Beacon ... 46 11. Error messages... 47

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Contents 12. Hygiene and maintenance... 50 General notes... 50 Limitations on processing... 51 Initial treatment at the point of use... 52 Manual cleaning... 53 Manual disinfection... 54 Automated cleaning and disinfection... 55 Drying... 56 Inspection, maintenance and testing... 57 Packaging... 58 Sterilization... 59 Storage...61 13. Servicing... 62 14. W&H accessories and spare parts... 64 15. Technical data... 67 16. Disposal... 69 W&H course certificate... 70 Explanation of warranty terms... 73 Authorized W&H service partners...74 Manufacturer’s declaration... 75

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Symbols

4

in the Instructions for Use

WARNING! (if persons could be injured)

ATTENTION! (if property could be damaged)

General explanations, without risk to persons or property

Thermo washer disinfectable

Sterilizable up to the stated temperature

Type B applied part (not suitable for intracardiac application)

Symbols Follow Instructions for Use

Class II equipment

Catalogue number

Date of manufacture

Foot control

Serial number

Do not dispose of with domestic waste

On / Off

Supply voltage of the control unit

DataMatrix code for product information including UDI (Unique Device Identification)

Electric fuse

Alternating current

Medical Device

Power consumption of the control unit

Earth

Supply current

CE marking XXXX with identification number of the Notified Body

25UX

on the control unit

MEDICAL – GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH ANSI/AAMI ES 60601-1:2005, ANSI/AAMI ES60601-1: A1:2012 + C1:2009/(R)2012 + A2:2010/(R)2012, CAN/CSA-C22.2 No. 60601-1:2008, CSA CAN/CSA-C22.2 NO. 60601-1:2014. 25UX – Control No.

Frequency of the alternating current Revolutions per minute (= rpm)

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Symbols

on the packaging

CE marking XXXX with identification number of the Notified Body

DataMatrix code for product information including UDI (Unique Device Identification)

This way up

Data structure in accordance with Health Industry Bar Code

Fragile, handle with care

+70 °C (+158°F) Max.

Temperature limitation

-40 °C (-40°F) Min.

Keep dry

80 %

Humidity, limitation

8%

»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 6

Caution! According to Federal law restricts this device to sale by or on the order of a physician, dentist, veterinarian or with the descriptive designation of any other practitioner licensed by the law of the State in which the practitioner practices to use or order the use of the device.

Symbols XXXX

on the irrigation tubing set

CE marking with identification number of the Notified Body

Not for re-use

Latex-free

Batch code

Use by

Sterilization with ethylene oxide

Catalogue number

Manufacturer

Keep away from heat

Do not resterilize

Do not use when package is damaged

DataMatrix Code for product information including UDI (Unique Device Identification)

Caution! According to Federal law restricts this device to sale by or on the order of a physician, dentist, veterinarian or with the descriptive designation of any other practitioner licensed by the law of the State in which the practitioner practices to use or order the use of the device.

Data structure in accordance with Health Industry Bar Code

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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 Mechanical drive unit with coolant supply for transmission instruments with ISO 3964 (DIN 13940) compatible coupling system, for use in dental surgery, implantology and maxillofacial surgery (CMF). Misuse may damage the medical device and hence cause risks and hazards for patients, users and third parties. Qualifications of the user Only suitably qualified medical, technical and specialist trained staff may use the medical device. We have based our developmed and design of the medical device 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 medical device when compliance with the following instructions is ensured: >> The medical device must be used in accordance with these Instructions for Use. >> The medical device has no components that can be repaired by the user. >> Modifications or repairs must only be undertaken by an authorized W&H service partner (see page 74). >> The electrical installation at the premises must comply with the regulations laid out in IEC 60364-7-710 (“Installation of electrical equipment in rooms used for medical purposes”) or with the regulations applicable in your country. >> Unauthorized opening of the control unit invalidates all claims under warranty and any other claims. In addition to unauthorized assembly, installation, modification of or repairs to the control unit, motor with cable, transmission instrument and non-compliance with our instructions, improper use will void the warranty and release us from all other claims. Any serious incident that has occurred in relation to the medical device should be reported to the manufacturer and the competent authority! 9

2. Electromagnetic compatibility (EMC) Medical electrical device is subject to particular precautions with regards to EMC and must be installed and put into operation in accordance with the EMC notes included. W&H only guarantees compliance of the device with the EMC Directives when it is used with original W&H accessories and spare parts. The use of accessories and spare parts that have not been approved by W&H may lead to increased emission of electromagnetic interference or to reduced resistance to 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. Unpacking  Remove the packaging.

 Remove the foot control, Instructions for Use and accessories.

 Remove the motor with cable.

 Lift out the insert with the control unit. Remove the mains cable, irrigant support, universal support, irrigation tubing set and Instructions for Use.

W&H packaging is environmentally friendly and can be disposed of by industrial recycling companies. However, we recommend that you keep the original packaging. 11

4. Scope of delivery SI-1023 (230V) 30288000

Control unit Irrigation tubing set 2.2 m (3 pcs, disposable) REF 07721800 Universal support REF 04005900 Irrigant support Mains cable country-specific REF 436360

Optional included in set EM-19 LC motor with electrical REF 30281000 contacts and 1.8 m cable EM-19 motor without electrical REF 30185000 contacts with 1.8 m cable REF 30264000 Foot control S-NW REF 30285000

Foot control S-N2

REF 07759700

CAN dongle

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SI-1015 (120V) 30289000 X X X X

SI-1010 (100V) 30290000

5. Safety notes

Control unit / Motor

>> Before using the medical device for the first time, store it at room temperature for 24 hours >> Check the medical device and the motor with cable for damage and loose parts every time before use. >> Do not operate the medical device and the motor with cable if it is damaged. >> Check the parameter settings every time the device is restarted. >> Perform a test run prior to every treatment. >> 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 medical device is not approved for operation in potentially explosive atmospheres. Do not twist or kink the motor cable! Do not coil it too tightly! Moisture in the motor with cable may cause a malfunction! (Risk of short circuit)

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Safety notes

Control unit

>> Use only original W&H fuses. >> Never touch the patient and the electrical connections on the control unit simultaneously. >> Make sure that no computer viruses are transferred to the control unit by an external data medium (USB stick). The connection of a USB hard drive with an external power source is not permitted. The control unit is classed as »conventional equipment« (closed equipment without protection against the ingress of water).

Use the WS-75 and WI-75 (20:1) ratios exclusively with the contra-angle handpieces approved by W&H. Use of other contra-angle handpieces may result in deviation from the indicated torque. The user alone is therefore responsible for the above. The manufacturer does not accept any liability.

Power failure In the event of a power failure, if the control unit is switched off, or when switching between programs, the last values set are saved and re-activated on power-up. System failure A total system failure does not constitute a critical fault. 14

Safety notes

Control unit / Motor

Mains cable / Power switch >> Only use the mains cable supplied. >> Plug the mains cable only into an earthed power socket. >> Set up the control unit so the power switch and the socket are easily accessible at all times. Disconnect the control unit from the power supply in case of danger. >> Turn off the control unit at the power switch. >> Pull the power plug out of the socket.

Rotational energy Deceleration of the bur can, cause the selected torque to be temporarily exceeded, compared to the value set, as a result of the rotational energy stored in the drive system. Observe the manufacturer’s speed and torque specifications for retaining screws for superstructures. Adjusting these retaining screws with an electric motor presents a potential risk as described above. Note that when using or setting low speeds, the operation or run-down of rotary instruments is more difficult to detect.

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Safety notes

Control unit / Motor / Foot control

Risks due to electromagnetic fields The functionality of implantable systems, such as cardiac pacemakers and implantable cardioverter defibrillator (ICD), can be affected by electric, magnetic and electromagnetic fields. >> Find out if patient and user have implanted systems before using the medical device and consider the application. >> Weigh the risks and benefits. >> Keep the medical device away from implanted systems. >> Do not place the motor on the patient’s body. >> Make appropriate emergency provisions and take immediate action on any signs of ill-health. >> Symptoms such as raised heartbeat, irregular pulse and dizziness can be signs of a problem with a cardiac pacemaker or ICD.

Foot control Follow the directions and safety notes in the Instructions for Use of the foot control. Foot control S-NW Keep the ORANGE button depressed to switch between the control units

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Safety notes

Coolant supply

The medical device is designed for use with physiological saline solution.

>> Always ensure correct operating conditions and that sufficient and adequate coolant is delivered. >> Always provide sufficient coolant and ensure the appropriate suction. >> Use only suitable coolants and follow the manufacturer’s medical data and instructions. >> Use the W&H irrigation tubing set or accessories approved by W&H.

Irrigation tubing set Sterile disposable irrigation tubing sets are supplied with the equipment. >> Note the expiration date and only use disposable irrigation tubing with undamaged packaging. >> Replace the disposable irrigation tubing immediately after every treatment. >> Follow your local and country-specific laws, directives, standards and guidelines for disposal.

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Safety notes Transmission instrument >> Follow the directions and safety notes in the Instructions for Use of the transmission instrument. >> Only use transmission instruments with an ISO 3964 (DIN 13940) compatible coupling system and manufacturer approved transmission instruments. >> Follow the directions of the manufacturer of transmission instrument with reference to transmission ratio, maximum speed and maximum torque.

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Safety notes Hygiene and maintenance prior to initial use >> Clean and disinfect the control unit, the motor with cable, the universal support and the irrigant support. >> Sterilize the motor with cable and the universal support.

Test run Do not hold the motor with transmission instrument at eye level. >> Connect the transmission instrument to the motor. Point the transmission instrument with the head facing downwards. >> Operate the motor with the foot control. >> In the event of operating malfunctions (e.g. vibrations, unusual noises or overheating), stop the motor immediately and contact an authorized W&H service partner.

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6. Description

of front panel

Pump cover

Display (touchscreen)

Irrigant support locator

Pump cover OPEN

Connection for motor

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