TS8X12

Organization name

MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

SRN

IT-MF-000026962

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

5 warnings recorded — scroll inside the panel to see all entries.

• CW011

  L’uso di questo dispositivo è controindicato nei pazienti con accertata ipersensibilità al silicone; a seconda della applicazione valutare se necessario sterilizzare il prodotto prima dell’uso; esaminare il prodotto attentamente prima dell’uso: non utilizzarlo in caso si riscontrino difetti.
• CW010

  EUDAMED did not publish a description for this code.
• CW009

  EUDAMED did not publish a description for this code.
• CW001

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

08033609521210

Basic UDI-DI

803360952DRENAGGIUH

Reference / catalog number

TS8X12

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Tubo in silicone "medical grade"

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 12 MU50
• 8 MU50

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

• A060299PERCUTANEOUS DRAINAGE SYSTEMS - OTHER