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KYRA MEDICAL KTEK2602 Manuel D'utilisation page 7

Sangles de nissen (bariatriques), sangles de sécurité pour patients

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  • FRANÇAIS, page 37
INSTRUCTIONS FOR USE
Cleaning and Disinfection:
WARNING:
After each use, clean the device as directed in this instruction for use.
Do not submerge the device in liquid. Equipment damage can occur.
Use caution in areas where liquid can get into the mechanism.
Do not use bleach or products that contain bleach to clean the device. Injury or equipment
damage can occur.
Make sure that the device is dry before you store it or use it again.
Wipes:
Wipes may contain up to 2% sodium hypochlorite.
o
Wipes may contain benzalkonium chloride (< or = 0.6% conc.) and didecyl dimethyl ammonium
o
chloride (up to 0.6% conc.)
Wipes may contain benzalkonium chloride (up to 0.6% conc.), didecyl dimethyl ammonium
o
chloride (up to 0.6% conc.) and may also contain polyhexamethylene biguanide (up to 0.6%
conc.).
Sprays:
Sprays may contain up to 2% sodium hypochlorite.
o
Sprays may contain up to .2% benzalkonium chloride and up to 0.2% didecyl dimethyl
o
ammonium chloride (quaternary ammonium chloride solution (QACs) and may also contain
polyhexamethylene biguanide (up to 0.6% conc.).
Sprays may contain up to 2% hydrogen peroxide.
o
Read the cleaning product's directions and follow the instructions on the label. Use caution in areas
where fluid migration may occur:
Wipe device with a clean, dry cloth. Make certain the product is dry prior to reinstalling to avoid damage.
CAUTION: Damage may result if product is cleaned with caustic chemicals or harsh abrasives
ATTENTION: If any KTEK product is damaged or appears to be functioning abnormally, discontinue use
and contact KYRA Customer Service at 1-508-936-3550.
4
Compliance with Medical Device Regulations:
This product is a non-invasive, Class I Medical Device and system is CE-marked according to
Annex VIII, Rule 1, of the Medical Device Regulations (REGULATION (EU) 2017/745).
EC Authorized
Representative:
Emergo Europe
Prinsessegracht 20
2514 AP The Hague,
Netherlands
Property of Kyra Medical, Inc. ©2021
Manufacturing
Information:
Kyra Medical, Inc.
102 Otis St
Northborough, MA 01532 USA
888-611-KYRA (North America)
508-936-3550 (International)
Page 6
EU Importer:
Kyra Medical Europe Limited
69 Esker Woods Drive
Lucan Co Dublin
K78PX45
Ireland
IFU Document Number: 03-0370-REV-F

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Ce manuel est également adapté pour:

Ktek2603Ktek2601