Skip to content

Aero-Med CA62475A

by Aero-Med LLC

Aero-Med CA62475A is a Class I device made by Aero-Med LLC, listed in FDA GUDID since 19 Oct 2026 (UDI-DI 10885380214516), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885380214516 UDI-DI Date19 Oct 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  • Withdrawn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
Aero-Med
Generic name
Urine specimen collection kit IVD
Model / Ref / Catalog
CA62475A
Primary DI / UDI-DI
10885380214516
FDA product code
OIB
GMDN term
Urine specimen collection kit IVD
Device class
Class I
Regulation number
864.3250
GUDID distribution status
In Commercial Distribution

Other devices from Aero-Med LLC

See all devices from Aero-Med LLC →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)