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Motionciser

by Guangzhou Xinbo Electronic Co., Ltd

Ref 09Model MC-001

Motionciser (09) is a vibration platform exerciser (EU MDR Class I; FDA Class I; FDA product code ISA, Massager, Therapeutic, Electric) made by Guangzhou Xinbo Electronic Co., Ltd, registered in EUDAMED on 29 May 2024 (Basic UDI-DI 697074222MCYR) and listed in FDA GUDID since 30 Jun 2025 (UDI-DI 06970742220339), active as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06970742220339 UDI-DI Date30 Jun 2025ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number697074222MCYR Basic UDI-DI 06970742220339UDI-DIDate29 May 2024RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 697074222MCYR registered 29 May 2024 Active
  • FDA GUDID UDI-DI 06970742220339 listed 30 Jun 2025 Listed

Timeline

2 dated events

  1. Registered EUDAMED 697074222MCYR
  2. Listed FDA GUDID 06970742220339

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  • Withdrawn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
Motionciser EUDAMED
Dr-Hos GUDID
Generic name
Vibration platform exerciser, stationary
Model / reference
MC-001 EUDAMED
09 EUDAMED
Motionciser GUDID
Primary DI / UDI-DI
06970742220339
Basic UDI-DI
697074222MCYR
FDA product code
ISA
EMDN code
V9099 Various devices not included in other classes - other
GMDN term
Vibration platform exerciser, stationary
Device class
Class I
Regulation number
890.5660
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MC-001
09
GUDID
Motionciser

Manufacturer details

EUDAMED SRN
CN-MF-000012183
Authorised representative
Share info GmbH DE-AR-000005132

Related devices

Category: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER.

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Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)