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Evermed CLF20LP

by Xiamen Taft 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06972077025313 UDI-DI Date6 May 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  • Withdrawn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
Evermed
Generic Name
Push-rim manual wheelchair, non-bariatric
Model / Reference
CLF20LP
Primary DI / UDI-DI
06972077025313
FDA Product Code
IOR
GMDN Term
Push-rim manual wheelchair, non-bariatric
Device Class
Class I
Regulation Number
890.3850
GUDID distribution status
In Commercial Distribution

Other devices from Xiamen Taft Medical Co., Ltd.

See all devices from Xiamen Taft Medical Co., Ltd. →

Properties

  • Lot / Batch Number
  • Serial 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
  • Premarket Exempt: No
  • Expiration Date: No