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Aquilavie J10047

by Ahc Americas LLC

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 Number10810118890588 UDI-DI Date27 Apr 2023ListedStatusListed 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  • Withdrawn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
Aquilavie
Generic name
Hypodermic needle, single-use
Model / Ref / Catalog
J10047
Primary DI / UDI-DI
10810118890588
FDA product code
MEG, FMF, FMI
GMDN term
Hypodermic needle, single-use
Device class
Class II
Regulation number
880.5860, 880.5570
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hypodermic needle, single-use

Other devices from Ahc Americas LLC

See all devices from Ahc Americas LLC →

Properties

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

Other properties (9)

  • 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