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Lower extremily intelligent feedback training system for children

by Guangzhou Yikang Medical Equipment Industrial Co., Ltd.

Ref A1miniSModel A1mini

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

CE MDR

Valid until

23 Jan 2030

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier SGS FIMKO OY

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number697534359A1miniX8 Basic UDI-DI 06975343590140UDI-DIDate27 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06975343590140 UDI-DI Date14 May 2026ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • FI25/1008008 Active Supplemented

    Quality management system EU MDR

    Certifier
    SGS FIMKO OY 0598
    Issued
    15 Jul 2026
    Expires
    23 Jan 2030
    Reason
    Add device or group

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  • Withdrawn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
Lower extremity intelligent feedback training system for children
Generic Name
Biomechanical function analysis system, force-testing, portable
Device Name
Lower extremily intelligent feedback training system for children
Model / Reference
A1mini EUDAMED
A1miniS EUDAMED
A1miniS Deer version GUDID
Primary DI / UDI-DI
06975343590140
Basic UDI-DI
697534359A1miniX8
Direct Marketing DI
06975343590140
FDA Product Code
IKK
EMDN Code
Z120602 Physiotherapy equipment
GMDN Term
Biomechanical function analysis system, force-testing, portable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
890.1925
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
A1mini
A1miniS
GUDID
A1miniS Deer version
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000031955
Authorised representative
Share info GmbH DE-AR-000005132

Other devices from Guangzhou Yikang Medical Equipment Industrial Co., Ltd

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Properties

  • Measuring Function
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: 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
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No