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Adapter

by Uniprox GmbH & Co.KG 71 variants

Part of a family of 71 devices: see the family page

Ref 41140800622000

Adapter (41140800622000) is a Class I device made by Uniprox GmbH & Co.KG, registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 4053646AdapterP7), active as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4053646AdapterP7 Basic UDI-DI 04053646000046UDI-DIDate9 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Adapter
Model / reference
41140800622000
Primary DI / UDI-DI
04053646000046
Basic UDI-DI
4053646AdapterP7
EMDN code
Y062412 Knee disarticulation prostheses
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000010327

Similar devices in this category

Other devices filed under KNEE DISARTICULATION PROSTHESES.

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Properties

Other properties (14, all answered No)