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Asp Medical MRT441

by Asp Global, LLC

Asp Medical MRT441 is a Class II device made by Asp Global, LLC, listed in FDA GUDID since 18 Sep 2020 (UDI-DI 00840216101661), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840216101661 UDI-DI Date18 Sep 2020ListedStatusListed 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  • Withdrawn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
Asp Medical
Generic name
Sputum specimen container IVD
Model / reference
MRT441
Primary DI / UDI-DI
00840216101661
FDA product code
BYZ
GMDN term
Sputum specimen container IVD
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sputum specimen container IVD

Similar devices

Other devices filed under FDA product code BYZ (Trap, Sterile Specimen).

Other devices from Asp Global, LLC

See all devices from Asp Global, LLC →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)