← Back to catalogue

Urgofilm

EUDAMED

Class I (EU MDR)

Ref 3664492012346

by Laboratoires URGO HEALTHCARE

Identity

Trade Name
URGOFILM EUDAMED
Device Name
URGOPLASTIC FILM TRANSPARENT EUDAMED
Model / Reference
3664492012346 EUDAMED

Identifiers

Primary DI / UDI-DI
03664492012346 EUDAMED
Basic UDI-DI
3664492LUHUS0011P6 EUDAMED
EMDN Code
H900299 TAPES, MEDICAL/SURGICAL - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Urgofilm by Laboratoires URGO HEALTHCARE — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
FR-MF-000001538

Sources (1)

  • EUDAMED 4fe1d89b-bf45-466f-9619-3f4107d09804 61 fields · synced Jun 18, 2026