QS-2B10

Trade name

not provided

06923646503107

69236465L56ZF

Reference / catalog number

QS-2B10

GS1

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

European Medical Device Nomenclature — the EU product classification assigned to this device.

• G03050101DIGESTIVE ENDOSCOPY, RETRIEVAL BALLOON DEVICES

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  1) This device is packaged and sterilized for single use only. Do not reuse, reprocess or re-sterilize. Reuse, reprocessing, or re-sterilization may compromise the structural integrity of the device and/or lead to device failure that in turn may result in patient injury, illness or death. Also, reprocessing or re-sterilization of single use devices may create a risk of contamination and/or cause patient infection or cross-infection, including, but not limited to, the transmission of infectious disease(s) from one patient to another. Contamination of the device may lead to injury , illness, or death of the patient 2)Do not use this device for any purpose other than stated intended use. 3)If the package is opened or damaged when received, do not use. Visually inspect with particular attention to kinks, bends and breaks. If an abnormality is detected that would prohibit proper working condition, do not use. Notify Leomed for return authorization. 4)Accordance with the laws and regulations, using of this device restricted to a trained professional physicians.