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FOURIER REHAB ArmMotus M2Pro

by Zhuhai Rehaconn Medical Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06980194220108 UDI-DI Date14 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Fourier Rehab
Generic Name
Continuous passive motion joint exerciser
Model / Reference
ArmMotus M2Pro
Primary DI / UDI-DI
06980194220108
FDA Product Code
IKK
GMDN Term
Continuous passive motion joint exerciser
Device Class
Class II
Regulation Number
890.1925
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Zhuhai Rehaconn Medical Co., Ltd.

Properties

  • Single Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No