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Urgofix

by Laboratoires URGO HEALTHCARE 3 variants

Ref 3664492001074, 3664292021270

Urgofix (3664492001074) is a Class I device made by Laboratoires URGO HEALTHCARE, registered in EUDAMED on 31 Dec 2021 (Basic UDI-DI 3664492LUHUS0012P8), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3664492LUHUS0012P8 Basic UDI-DI Date31 Dec 2021RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
3664492001074, 3664292021270
Primary DI / UDI-DI
03664492001074, 03664492021270
Basic UDI-DI
3664492LUHUS0012P8
Direct marketing DI
03664492001074
03664492021270
EMDN code
H900299 Tapes, medical/surgical - other
Device class
Class I
EU registration type
Standard device
EU market of registration
France
Bulgaria

Manufacturer details

EUDAMED SRN
FR-MF-000001538

Similar devices in this category

Other devices filed under TAPES, MEDICAL/SURGICAL - OTHER.

Other devices from Laboratoires URGO HEALTHCARE

See all devices from Laboratoires URGO HEALTHCARE →

Properties

  • Contains animal tissues or cells
Other properties (13, all answered No)