background image

20 

                                                                                                                           

KFISH/01/19.11.2018 

                                                   

 

 

14.

 

Symbols and Descriptions 

 

 

 1984 

This device complies with the requirements of the Medical Devices 
Directive(93/42/EEC) 

 

Manufacturer 

 

Date of Manufacture 

 

Class II Equipment per IEC 60601-1 

 

Type B Applied Part per IEC 60601-1 

 

Consult instructions for use 

 

LOT Number 

 

Model Number 

 

Serial Number 

 

Disposal of Electrical & Electronic Equipment (WEEE): 
Do not treat this product as household waste. 

 

 

 

21 

                                                                                                                           

KFISH/01/19.11.2018 

                                                   

 

15.

 

Device & Outside Box’s Symbols 

Descriptions 

 

Warning/Caution/Note 

 

Keep Away From Sunlight 

 

Keep Away From Getting Wet 

 

Handle With Care 

 

Rohs Declaration 

 

Barcode Number 

 

16.

 

European Conformity Mark 

Notified Body: KIWA Belgelendirme Hizmetleri A.Ş. (1984)

 

The product conforms to European Medical Device 

Directive (93/42/EEC) and meets applicable health, safety 

and environmental requirements. If the mark is 

accompanied by a number, conformity is verified by the 

indicated notified body. 

17.

 

Manufacturer and Technical Service Information 

 

Hünkar Ecza ve Medikal San. Tic. Ltd. Şti.

 

Akçeşme Mahallesi 2019 sk. No:5 Merkezefendi

 

Denizli /TÜRKİYE

 

Tel: +90 258 371 46 56 

www.hunkarmedikal.com

 

 

1984 

Содержание HNK-NBL-FISH

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Страница 2: ...lar kullan n z Orijinal aksesuarlar d nda ve kullan c n n ki isel sebeplerinden kaynaklanan hasarlar i in garanti hizmeti sa lanmaz Cihaz kullanmadan nce t m aksesuarlar n al r vaziyette oldu undan em...

Страница 3: ...la kab ila kab kapa ve a zl k par alar n kaynar su i inde 10 dakika bekletin 3 Yeti kin maskesi ve ocuk maskesi ise sirke saf su kar m i erisinde tamamen bat r lacak ekilde 30 dakika bekletilir 4 Daha...

Страница 4: ...kullan l p kullan lmad n kontrol ediniz F Hava hortumun katlan p katlanmad n kontrol ediniz F Cihaz hava filtresi t kanm olabilir kontrol ediniz Cihaz a r derecede s n yor F Cihaz havaland rma kanall...

Страница 5: ...z aras ndaki ISM frekans bantlar n n ve 80 MHz ila 2 5 GHz aras ndaki frekans aral n n uygunluk seviyeleri mobil ta nabilir ileti im ekipmanlar n n yanl l kla hastan n bulundu u alana getirildi inde e...

Страница 6: ...3 EMC Electromagnetic Compatibility Decalaration 16 14 Symbols and Descriptions 20 15 Device Outside Box s Symbols Descriptions 21 16 European Conformity Mark 21 17 Manufacturer and Technical Service...

Страница 7: ...ieces which can go down easily This device shouldn t use in the enviroment where inflammable gases oxygen and aerosol sprays used in This device is used for breathing passage treatment under the contr...

Страница 8: ...r which is not boiled and clean the pieces Less than 50 C Don t wash the device s main unit air tube and air filter 1 Take out the device s mouthpiece mask medication cup and air tube 2 Empty the resi...

Страница 9: ...4 Test 5 Test 14 KFISH 01 19 11 2018 10 Keeping and Transporting The device can be kept with its package in well aired room humid is not more than 10 95 and the temperature between 25 70 C Under this...

Страница 10: ...uld be at levels characteristic of a typical location in a typical commercial or hospital environment Note Ut is the AC mains voltage prior to application of the test level 18 KFISH 01 19 11 2018 Guid...

Страница 11: ...ox s Symbols Descriptions Warning Caution Note Keep Away From Sunlight Keep Away From Getting Wet Handle With Care Rohs Declaration Barcode Number 16 European Conformity Mark Notified Body KIWA Belgel...

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