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Universal Joint Adult

by Hugh Steeper Limited 2 variants

Ref B00774

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50553482HSH000BG Basic UDI-DI 50553482588092UDI-DIDate12 May 2022RegisteredStatusActive

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  • Withdrawn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
Split-hook/specialized-tool hand prosthesis
Model / Reference
B00774
Primary DI / UDI-DI
50553482588092
Basic UDI-DI
50553482HSH000BG
EMDN Code
Y061899 Upper extremity prostheses - other
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
GB-MF-000010196
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Hugh Steeper Limited

See all devices from Hugh Steeper Limited →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No