E-Swin E-Eye User Manual Download Page 23

44

45

MARKING

TECHNICAL CHARACTERISTICS

 RECYCLING AND PROCESSING

Instructions for the processing of end-of-life products: the WEEE Directive (Waste Electrical and  

Electronic Equipment) 2020/96/EC has been implemented to ensure that products are recycled by the 

application of optimum techniques for processing, exploitation and recycling, thereby contributing to 

the protection of the environment and human health. 

Your product has been designed and manufactured using high-quality products, which are suitable 

for recycling and re-use. 
E-Swin SAS is affiliated to an eco-organization, which undertakes the collection and processing of 

end-of-life products.

 SPECIFICATIONS

Technology

IRPL

®

 

(Intense Regulated Pulsed Light)

.

Wavelength

>

 580 nm

Charging time / energy source

Continous operation

Dimensions (L x W x H)

Max 345 x 320 x 440 mm

Weight

Max 11,5kg

.

Shipping box dimensions (L x W x H)

Max 740 x 460 x 610 mm

Shipping weight

Max 17,5kg

Noise level

Max 55 dBA

Operating voltage

100 - 240 VAC

Maximum power consumption

540 VA

Frequency

50/60 Hz

Temperature

Operating: +5 to +25°C
Storage: -5 to +65°C

Relative working humidity (non-condensing)

30 - 93 %

Atmospheric pressure

70-106 kPa

 MARQUAGE

:

 

Reference to the treatment of meibomian blepharitis (dry-eye syndrome) using 

 device.

......................

Unique serial number of your 

 

E-SWIN

Rue des Côtes d´Orval

ZA de la Prévôté

78550 Houdan - FRANCE

Year of manufacture of your device and address of the manufacturer.

0197

Medical  device  conforming  to  requirements  of  the  European  Directive  93/42/CEE,  certified  by  an 

independent body.

IP 2X

Device protected against solid foreign body of 12,5 mm in diameter or more (IP rating).

Functional grounding terminal.

Logo corresponding to a degree of protection against electric shock for parts that are applied onto the 

patient (Part to be applied - Type BF).
Electromedical device of Class II rating.

Device must be used indoors.

Keep the device dry.

Keep away from light and heat.

User manual.

It is compulsory to refer to the instructions in the user manual.

100 - 240 V~ 50-60 Hz

540 VA

Operating conditions - supply voltage (alternating current), frequency of the mains voltage, power.

Warning, dangerous voltage device.

Global safety mark for electronical devices.

Optical radiation aperture

Respect upper and lower temperature limits indicated beside this logo.

Do not use this product after the deadline specified beside this logo (

gel

).

The batch number of the product is indicated beside this logo (

gel

).

Warning label according to IEC60601-2-57:2011

Summary of Contents for E-Eye

Page 1: ...User Manual...

Page 2: ...nging and is a practical example of this fact Your patients can now enjoy the benefits of a new treatment for meibomian blepharitis dry eye syn drome using state of the art pulsed light technology wit...

Page 3: ...ETC The manufacturer s guarantee for parts and labour will only be valid if your device is returned in its complete original packaging All items of original packaging in which your was delivered shou...

Page 4: ......

Page 5: ...onal user of must ensure that only persons who fulfil the criteria for use described in the present manual will receive treatment using Before using your the following information should be read caref...

Page 6: ...lement for less than two months On an injured burned or infected skin On skin lesions of unusual appearance which will require investigation On high risk areas blemishes birthmarks warts unhealed woun...

Page 7: ...nection Activation card slot Applicator holding Ventilation grid Visor to protect touchscreen Mobile head Release clips for the mobile head Mobile head Applicator zone Applicator zone Air vents Trigge...

Page 8: ...use of the device 13 Pause icon for the flash treatment session pressing this icon will place in pause mode In this mode no flash can be emitted from the applicator To exit this mode press the same i...

Page 9: ......

Page 10: ...plicator photo 3 Push the extractor into the mobile head to its full length photo 4 Apply pressure simultaneously to the 2 retaining lugs of the mobile head and remove the mobile head photo 5 Remove t...

Page 11: ...nce entered these codes will not be requested a second time Connect using the mains lead The internal test procedure of will commence and will last for a few seconds Upon the completion of this phase...

Page 12: ...n a generous layer minimum 1cm thick on the cheekbone and the tempo ral areas making sure that the gel does not get under the eye mask Locate your mask goggles and put them on If there are other perso...

Page 13: ......

Page 14: ...tivation card and its optic cartridge must be replaced when the number of flashes reaches zero STAGE 2 COOLING OF OPTICAL PARTS During the procedure for the replacement of the optic cartridge before s...

Page 15: ...tridges are not symmetrical so they must be inserted in the right sense and certainly not in the other Check that the cartridge is correctly engaged PRECAUTIONS throughout the procedure for the replac...

Page 16: ...the old activation card and insert the new card supplied with the optic cartridge in the slot provided for this purpose photo I Each activation card carries the same serial number as the optic cartrid...

Page 17: ...on icon 7 The C key can be used to correct the figure in each box SELECT LANGUAGE screen L Click on the flag which corresponds to the required language The Language change confirmed message will be d...

Page 18: ......

Page 19: ...o danger or entail the risk of irreparable damage to your device Once o p t i c cartridge is removed it should be handled by the plastic parts only above all the electrodes the tube or the reflector s...

Page 20: ...sothiazolinone 0 05 0 15 Deionized water Q S 100 For external use only Not to be used on broken burned or infected skin Keep out of reach of children The tool extractor is used for the separation of t...

Page 21: ...of your device Never apply the clean spray directly to the internal components of the applicator APPLICATOR BODY All plastic components of the applicator must be cleaned using a clean cloth which has...

Page 22: ...ols of the optical parts of the applicator to end SECU 03 SECU 04 SECU 05 SECU 07 SECU 09 Your device is blocked Contact our technical department by filling out the contact form on www esw vision com...

Page 23: ...pheric pressure 70 106 kPa MARQUAGE Reference to the treatment of meibomian blepharitis dry eye syndrome using device Unique serial number of your E SWIN Rue des C tes d Orval ZA de la Pr v t 78550 Ho...

Page 24: ...considered If the measured field strength in the location in which the device is used exceed the applicable RF compliance level above the device should be observed to verify normal operation If abnor...

Page 25: ...or the applicator as you may risk exposure to high voltages Never use cartridges and acces sories other than those designated and sold by E Swin SAS for use with ENVIRONMENTAL PROTECTION You must abi...

Page 26: ...ns described in this manual will invalidate the guarantee The company E Swin SAS will not accept liability for any accident arising from failure to observe the instructions contained in this manual or...

Page 27: ...0197 ZA de la Pr v t Rue des C tes d Orval 78550 Houdan FRANCE 01 30 46 37 61 www esw vision com M029GB000F08A rev F 2021 06 11...

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