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RemoHip 801942400

by Hangzhou Rejoin Mastin Medical Device Co., Ltd.

Ref 801942400

RemoHip 801942400 is a Class I device made by Hangzhou Rejoin Mastin Medical Device Co., Ltd., registered in EUDAMED on 22 May 2026 (Basic UDI-DI 69418325P2021036199J) and listed in FDA GUDID since 22 May 2023 (UDI-DI 06973877662708), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number69418325P2021036199J Basic UDI-DI 06973877662708UDI-DIDate22 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06973877662708 UDI-DI Date22 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 69418325P2021036199J registered 22 May 2026 Active
  • FDA GUDID UDI-DI 06973877662708 listed 22 May 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 06973877662708
  2. Registered EUDAMED 69418325P2021036199J

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
RemoHip
Generic name
Arthroscopic surgical procedure kit, non-medicated, reusable
Device name
Reusable Surgical Instruments
Model / reference
801942400
Primary DI / UDI-DI
06973877662708 EUDAMED
06973877662852 GUDID
Basic UDI-DI
69418325P2021036199J
Direct marketing DI
06973877662708
FDA product code
HWL
EMDN code
L1909 Arthroscopic surgery scalpels, meniscotomes and knives reusable
GMDN term
Arthroscopic surgical procedure kit, non-medicated, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
06973877662708
GUDID
06973877662852

The registries describe this device under different primary UDI-DIs (EUDAMED lists 06973877662708; FDA GUDID lists 06973877662852), so their flags are not compared.

Related devices

Category: Arthroscopic surgical procedure kit, non-medicated, reusable

Similar devices in this category

Other devices filed under ARTHROSCOPIC SURGERY INSTRUMENTS, REUSABLE.

Other devices from Hangzhou Rejoin Mastin Medical Device Co., Ltd.

See all devices from Hangzhou Rejoin Mastin Medical Device Co., Ltd. →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)