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Aira 100205

by Aira, LLC

Aira 100205 is a Class I device made by Aira, LLC, listed in FDA GUDID since 16 Jan 2026 (UDI-DI 00810194401640), 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 Number00810194401640 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  • Withdrawn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
Non-woven gauze pad
Model / reference
100205
Primary DI / UDI-DI
00810194401640
FDA product code
NAB
GMDN term
Non-woven gauze pad
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Similar devices

Other devices filed under FDA product code NAB (Gauze / Sponge,Nonresorbable For External Use).

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

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)