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Aero-Med

by Aero-Med LLC 20 variants

Aero-Med (QUE3525) is a Class I device made by Aero-Med LLC, listed in FDA GUDID since 11 Sep 2025 (UDI-DI 00810010894892), registry data as of 8 Jun 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 8 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810010894892 UDI-DI Date11 Sep 2025ListedStatusListed 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  • Withdrawn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

Generic name
General specimen container IVD, additive/medium
Model / Ref / Catalog
QUE3525
Primary DI / UDI-DI
00810010894892
FDA product code
NNK
GMDN term
General specimen container IVD, additive/medium
Device class
Class I
Regulation number
864.3250
GUDID distribution status
In Commercial Distribution

Related devices

Category: General specimen container IVD, additive/medium

Similar devices

Other devices filed under FDA product code NNK (CONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE).

Other devices from Aero-Med LLC

See all devices from Aero-Med LLC →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)