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Crutch

by Rehand Medical Technology Co. Ltd.

Ref 06977342170019Model RH1101,RH1106,RH1201,RH1301,RH1401,RH1501,RH1601,RH1701,RH1811,RH1815,RH1901,RH1A01,RH1C01,RH1D21

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6977342170002AU Basic UDI-DI 06977342170002UDI-DIDate6 Jul 2024RegisteredStatusActive

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  • Withdrawn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
RH1101, RH1106, RH1201, RH1301, RH1401, RH1501, RH1601, RH1701, RH1811, RH1815, RH1901, RH1A01, RH1C01, RH1D21, 06977342170019
Primary DI / UDI-DI
06977342170002
Basic UDI-DI
6977342170002AU
Direct Marketing DI
06977342170002
EMDN Code
Y12030601, Y12030602, Y12030603
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000038451
Authorised representative
Umedwings Netherlands B.V. NL-AR-000000444

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