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Ace 0.22*40

by Wuxi Jiajian Medical Instrument Co., Ltd. 5 variants

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 Number06972011712309 UDI-DI Date10 Jun 2020ListedStatusListed 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  • Withdrawn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
Ace
Generic name
Acupuncture needle, single-use
Model / reference
0.22*40
Primary DI / UDI-DI
06972011712309
FDA product code
MQX
GMDN term
Acupuncture needle, single-use
Device class
Class II
Regulation number
880.5580
GUDID distribution status
In Commercial Distribution

Related devices

Category: Acupuncture needle, single-use

Other devices from Wuxi Jiajian Medical Instrument Co., Ltd.

See all devices from Wuxi Jiajian Medical Instrument Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date

Other properties (10)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No