Skip to content

none AX35

by Zhejiang Mateside Medical Devices Technology 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 Number06975960550558 UDI-DI Date29 Sep 2025ListedStatusListed 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  • Withdrawn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
none
Generic Name
Stand-assistive attendant-only-propelled wheelchair
Model / Reference
AX35
Primary DI / UDI-DI
06975960550558
FDA Product Code
FNG
GMDN Term
Stand-assistive attendant-only-propelled wheelchair
Device Class
Class II
Regulation Number
880.5500
GUDID distribution status
In Commercial Distribution

Other devices from Zhejiang Mateside Medical Devices Technology Co., Ltd

See all devices from Zhejiang Mateside Medical Devices Technology Co., Ltd →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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