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Aira 119304

by Aira, LLC

Aira 119304 is a Class I device made by Aira, LLC, listed in FDA GUDID since 16 Jan 2026 (UDI-DI 00810194400193), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810194400193 UDI-DI Date16 Jan 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Aira
Generic name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
119304
Primary DI / UDI-DI
00810194400193
FDA product code
LZA
GMDN term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LZA (Polymer Patient Examination Glove).

Other devices from Aira, LLC

  • Aira 119132

    Class I

  • Aira 119133

    Class I

  • Aira 119134

    Class I

  • Aira 119144

    Class I

See all devices from Aira, LLC →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)