Država: Bjelorusija
Jezik: ruski
Izvor: Министерством здравоохранения Республики (Центр экспертиз и испытаний в здравоохранении)
SUMI spolka z ograniczona odpowiedzialnoscia sp. k., ПОЛЬША
изделия медицинского назначения
SUMI spolka z ograniczona odpowiedzialnoscia sp. k.
2023-06-05
f~F] catalogue number ~ manufacturer ~ serial No. I~~~~”dI CO Steritized by ethylene snide ~ date of manufacture latex-free ~ use by [Jj~] consut instnjcbons for use the product comples with the requirements of tire European Caution: read all warnings C E 1011 UnioniNumber of the Nstitied 9~y and precautions in ~ instructions for use participating in the device conformity assessment ~ free from phthalates (ind. DEHP) keep dry —4- do not use if packaging —„~ ~ is damaged krep away from sunlight ~ do not resterilize ~~r~0”i store at 5-40 C Introduction Tire instructions are intended for doctors, nursing staff and the patient (hereinafter referred to as the usero), in order to ensure safe and correct use of KAN tracheostomy tubes both in healthcare facilities and in domestic conditions. Read tire instruction for use before first use of the devicel The packaging of the fracheostomy tube must be kept for the entire pesod the tube iu used duetu tire identitcation dala and the device data oo the labe Users have tu be trained by profess ona medica station the use of the device KAN tracheostomy tubes and KAN trachesotumy short tubes from SUMI are intended for use only by one patient Multiple uses of the device for sue and the same patient are allowed. The maximum usage time of one tube will not exceed 29 days. It is recommended that tire tubes be replaced and cleaned frequently, especially interna canoulas Preferably by medical staff. If damages, cracks or deformation occur during handling, replace the tube or damaged component. Damaged device components or tubes must not be used. In order to avoid contusion with tube selection and easier identitcatiun each tube size is mailied with a suitable color print on the ffange. The device is lutes free. The device in its original, undamaged packaging is stenlized by ethylene oxide The device must not be restenlized This instruction for ase appties only to the following sets of tracheontomy tubes: KAN tracheostomy tube without cuff, REF 47 osOO 47-axOl KAN tracheostomy t Pročitajte cijeli dokument