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571 Noir

by Vilgo

Part of a family of 18 devices: see the family page

Ref 1020013S12

571 Noir (1020013S12) is a Class I device made by Vilgo, registered in EUDAMED on 3 Dec 2025 (Basic UDI-DI 361580571PA), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number361580571PA Basic UDI-DI 03615800008612UDI-DIDate3 Dec 2025RegisteredStatusActive

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  • Withdrawn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

Device name
571
Model / reference
1020013S12
Primary DI / UDI-DI
03615800008612
Basic UDI-DI
361580571PA
Direct marketing DI
03615800008612
EMDN code
Y12030601 Elbow crutches
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000009712

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Properties

Other properties (14, all answered No)