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Results of the electromagnetic tests

Requirement

Class / Test Level*

Electromagnetic emissions

Mains terminal disturbance voltage (Conducted Emissions)

CISPR 11/EN 55011 [150 kHz – 30 MHz]

Group 1

Class B

Electromagnetic radiation disturbance (Radiated Emissions)

CISPR 11/EN 55011 [30 MHz – 1000 MHz]

Group 1

Class B

Harmonic distortion IEC/EN 61000-3-2

Class A

Voltage fluctuations and flicker IEC/EN 61000-3-3

 –

Immunity to electromagnetic interference

Electrostatic discharge (ESD)

IEC/EN 61000-4-2

Contact discharge: ±2 kV, ±4 kV, ±6 kV, ±8 kV

Air discharge: ±2 kV, ±4 kV, ±8 kV, ±15 kV

Radiated RF electromagnetic fields

IEC/EN 61000-4-3 [80 MHz – 2.7 GHz]

10 V/m

Proximity fields from RF wireless communications equipment

IEC/EN 61000-4-3

710 / 745 / 780 / 5240 / 5500 / 5785 MHz

9 V/m

385 MHz

27 V/m

450 / 810 / 870 / 930 / 1720 / 1845 / 1970 / 2450 MHz

28 V/m

Electrical fast transients / bursts 

IEC/EN 61000-4-4

Mains supply: ±2 kV

Surges IEC/EN 61000-4-5

±1 kV L – N

±2 kV L – PE

±2 kV N – PE

Conducted disturbances induced by RF fields

IEC/EN 61000-4-6

3 V

6 V in ISM bands and in amateur radio bands

Power frequency magnetic fields IEC/EN 61000-4-8

30 A/m

Voltage dips, short interruptions and voltage variations  

IEC/EN 61000-4-11

   0%

   0%

70%

   0%

for 0.5 cycle at 45° steps from 0°-315°

for 1 cycle

for 25/30 cycles

for 250/300 cycles

Proximity magnetic fields

IEC/EN 61000-4-39

30 kHz

8 A/m

134.2 kHz

65 A/m

13.56 MHz

7.5 A/m

* There are no deviations or simplifications to IEC/EN 60601-1-2.

Summary of Contents for proxeo TWIST

Page 1: ...Instructions for use PL 40 H...

Page 2: ...Charging the battery 19 Query battery status 20 Pairing 21 Assembly removal of the Prophy Angle 23 6 Handpiece drive 24 Switch on off 24 Test run 25 7 Hygiene and maintenance 26 General notes 26 Limit...

Page 3: ...cing 38 10 Accessories consumables spare parts and other recommended medical devices by W H 40 11 Technical data 41 12 Data on electromagnetic compatibility according to IEC EN 60601 1 2 44 13 Disposa...

Page 4: ...ollow instructions for use Manufacturer Date of manufacture CE mark with identification number of the Notified Body XXXX Medical device Thermo washer disinfectable Sterilizable up to the stated temper...

Page 5: ...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...

Page 6: ...6 Symbols l RCM Australian New Zealand GITEKI MIC Japan ANATEL Brazil FCC IC USA Canada R 209 J00204...

Page 7: ...t importance to us Observe the safety notes Intended use PL 40 H Battery driven electrical drive unit with wireless foot controller to perform cleaning and polishing of tooth surfaces and fillings Mis...

Page 8: ...irs must only be undertaken by an authorized W H service partner see page 49 The electrical installation at the premises must comply with the regulations laid out in IEC 60364 7 710 Installation of el...

Page 9: ...9 2 Scope of delivery REF Description 30317000 Handpiece drive 07969610 Charger with adaptor 05882600 Handpiece holder Optional included in set 30316000 Foot control C NW with Stick...

Page 10: ...contacts on the medical device simultaneously Only put the medical device into operation when the handpiece sleeve is attached Do not expose the medical device to any violent mechanical impacts Batter...

Page 11: ...evice is not approved for operation in potentially explosive atmospheres Charger Only use chargers approved by W H Hygiene and maintenance prior to initial use Clean and disinfect the medical device S...

Page 12: ...cardiac pacemaker of at least 15 cm 5 9 inch is maintained The functionality of other active implantable medical devices AIMD e g ICD can be affected by electric magnetic and electromagnetic fields F...

Page 13: ...1 83 m 1 83 m The patient environment see diagram encompasses the area up to 2 50 m above the patient and 1 83 m in all horizontal directions The charger must not be used within the patient environmen...

Page 14: ...w the operating instructions of the manufacturer Insert the Prophy Angle only when the medical device is stationary Never touch the Prophy Angle while it is still rotating Only use Prophy Angles with...

Page 15: ...15 4 Description Handpiece drive ON OFF button Handpiece sleeve Charging socket Coupling for Prophy Angle Nose Status LED handpiece drive see page 17 Status LED foot control see page 18...

Page 16: ...16 Description Foot control C NW Charging LED orange see page 18 19 Status LED green see page 18 21 Reset button Pairing button Charging socket Stick...

Page 17: ...ORANGE e Battery is charging Not ready for operation e Battery is 2 25 charged Complete the treatment Do not start any further treatment Charge the battery e Battery is 1 charged Charge the battery R...

Page 18: ...ooting with pairing problems see page 22 The LED flashes for 40 milliseconds every 4 seconds Standby mode The foot control can be activated by pressing LED steady steady flashes flashes intermittently...

Page 19: ...rst time Insert the charging cable into the handpiece drive charging socket until it audibly engages Plug the charger into an power socket Connect the charging cable into the foot control charging soc...

Page 20: ...tus LED flashes Battery status 3 x green 75 100 2 x green 50 75 1 x green 25 50 orange 2 25 Briefly press the ON OFF button You can query the battery status when the handpiece drive is switched on and...

Page 21: ...ce drive are already paired when delivered If pairing is active Status LED green flashes on the foot control Both devices need to be in pairing mode for it to be possible to pair the handpiece drive a...

Page 22: ...the position of the foot control Eliminate any sources of interference e g brush motors mobile telephones radios WLAN Use the stick to press the reset button on the foot control and try pairing again...

Page 23: ...rophy Angle Cup or Brush Position the groove on the Prophy Angle with the nose of the handpiece drive Push the Prophy Angle onto the handpiece drive until the limit stop Verify full engagement Hold th...

Page 24: ...rol as far as it will go to attain the maximum speed of 3 000 rpm The following light signals are shown on the foot control Foot control pressed Status LED green flashes Foot control is attempting to...

Page 25: ...level Attach the Prophy Angle to the handpiece drive Operate the handpiece drive with the foot control In the event of operating malfunctions e g vibrations unusual noise overheating stop the medical...

Page 26: ...s 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 e...

Page 27: ...rmined 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...

Page 28: ...ire handpiece drive the handpiece sleeve and the handpiece holder with disinfectant Ensure that no fluids enter the medical device Switch the handpiece drive off The charger must not be connected Note...

Page 29: ...the handpiece drive s basic suitability for effective manual cleaning was provided by an independent test laboratory using tap water 35 C and towels cloth WIPEX WET DESI premium NORDVLIES GmbH Bargteh...

Page 30: ...the handpiece drive the handpiece sleeve and the handpiece holder for effective manual disinfection was provided by an independent test laboratory using the mikrozid AF wipes disinfectant Sch lke Mayr...

Page 31: ...handpiece holder are not approved for automated processing in a washer disinfector and sterilization Evidence of the handpiece sleeve s basic suitability for effective automated disinfection was prov...

Page 32: ...32 Hygiene and maintenance Ensure that the medical device is completely dry internally and externally after cleaning and disinfection Remove any liquid residues using compressed air Drying...

Page 33: ...vice after cleaning and disinfection for damage visible residual soiling and surface changes Reprocess any medical devices that are still soiled Sterilize the handpiece sleeve following cleaning and d...

Page 34: ...following requirements The sterilization package must meet the applicable standards in respect of quality and use and must be suitable for the sterilization method The sterilization package must be l...

Page 35: ...s Maximum sterilization temperature 135 C 275 F Evidence of the handpiece sleeve s basic suitability for effective sterilization was provided by an independent test laboratory using the LISA 517 B17L...

Page 36: ...36 Handpiece sleeve Store sterile goods dust free and dry The shelf life of the sterile goods depends on the storage conditions and type of packaging Hygiene and maintenance Storage...

Page 37: ...ing Pull the handpiece sleeve off the handpiece drive Squeeze the O ring between your thumb and index finger firmly so that it forms a loop Pull the old O ring off Push the new O ring on in its place...

Page 38: ...tion and safety of the medical device is necessary and should be carried out at least once every three years unless shorter intervals are prescribed by law The periodic inspection covers the complete...

Page 39: ...mmediately contact an authorized W H service partner Repairs and maintenance work must only be undertaken by an authorized W H service partner Ensure that the medical device has been completely proces...

Page 40: ...882600 Handpiece holder 07918800 Handpiece sleeve 07969610 Charger incl adaptor 30316000 Foot control C NW with Stick 02695700 O ring 3 pcs 07979710 Prophy Angle Cup 105 firm dark green 100 pcs 079949...

Page 41: ...voltage 3 7 V Rated capacity 680 mAh Max speed 3 000 rpm Maximum torque 2 Ncm Dimensions WxDxH 160 x 25 x 28 mm Weight 118 g Ambient conditions Temperature during storage and transport 20 C bis 60 C...

Page 42: ...ger Rated voltage 100 240 V Permissible voltage fluctuation 10 Frequency 50 60 Hz Power 7 VA Freuquency band 2 4 GHz ISM band 2 402 2 480 GHz Transmitting power 3 dBm Modulation GFSK Channels 40 chann...

Page 43: ...t not suitable for intracardiac application Classification according to Paragraph 6 of the General Specifications for the Safety of Medical Electrical Equipment according to IEC 60601 1 ANSI AAMI ES 6...

Page 44: ...ser should assure that this medical device is set up and used in an environment of the specified type and or in accordance with the specifications of the manufacturer This medical device uses RF energ...

Page 45: ...ts 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 Use of t...

Page 46: ...3 80 MHz 2 7 GHz 10 V m Proximity fields from RF wireless communications equipment IEC EN 61000 4 3 710 745 780 5240 5500 5785 MHz 9 V m 385 MHz 27 V m 450 810 870 930 1720 1845 1970 2450 MHz 28 V m...

Page 47: ...13 Disposal Ensure that the parts are not contaminated on disposal Follow your local and national laws directives standards and guidelines for disposal Medical device Waste electrical equipment Packag...

Page 48: ...is liable for material or manufacturing defects within a warranty period of 12 months from the date of purchase Accessories and consumables handpiece holder stick are excluded from the warranty We ac...

Page 49: ...49 Authorized W H service partners Find your nearest authorized W H service partner at http wh com Simply go to the menu option Service for full details Or simply scan the QR code...

Page 50: ...W H Dentalwerk B rmoos GmbH Ignaz Glaser Stra e 53 5111 B rmoos Austria t 43 6274 6236 0 f 43 6274 6236 55 office wh com wh com Form Nr 50928 AEN Rev 009 17 07 2023 Subject to alterations...

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