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Sleeve Remover

by Shanghai Sanyou Medical Co., Ltd.

Ref 31101101, 30125041

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06936968857278 Basic UDI-DI Date13 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Sleeve Remover
Model / Reference
31101101, 30125041
Primary DI / UDI-DI
06936968857278, 06941977563133
Basic UDI-DI
B-06936968857278, B-06941977563133
EMDN Code
L0919 Orthopaedic and traumatological surgery instrument kits, reusable
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000004488
Authorised representative
Wellkang Ltd XI-AR-000001836

Other devices from Shanghai Sanyou Medical Co., Ltd.

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Properties

  • Reusable

Other properties (10)

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