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Adapter

by Uniprox GmbH & Co.KG 71 variants

Part of a family of 27 devices: see the family pagePart of a family of 71 devices: see the family page

Ref 41140200022000, 41140200022000neu

Adapter (41140200022000) is a Class I device made by Uniprox GmbH & Co.KG, registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI 40536464AdapterGB), 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 Number40536464AdapterGB Basic UDI-DI 04053646000251UDI-DIDate16 Jul 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  • Withdrawn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
41140200022000, 41140200022000neu
Primary DI / UDI-DI
04053646000251
Basic UDI-DI
40536464AdapterGB, 4053646AdapterP7
EMDN code
Y062409, Y062412, Y062415
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000010327

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Properties

Other properties (14, all answered No)