UTM

Trade name

UTM

UDI-DI code

18053326003216

Basic UDI-DI

80533260BD0260AM0049D

Reference / catalog number

365C

Issuing entity

GS1

Risk category

IVDR Class A

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

UTM KIT 2 mL, Medium + Pernasal Flocked Swab

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.

• W050301020101SAMPLES ANALYSES, PLASTIC TUBES WITH ADDITIVES

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

• CW009

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

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.

No certificate specifically references this device's Basic UDI-DI.