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Vial Set ASPP99DPTVL

by Argon Medical Devices, Inc.

Vial Set ASPP99DPTVL is a general laboratory container (FDA Class I; FDA product code FMH, Container, Specimen, Sterile) made by Argon Medical Devices, Inc., listed in FDA GUDID since 19 Jul 2022 (UDI-DI 00886333220984), 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 Number00886333220984 UDI-DI Date19 Jul 2022ListedStatusListed 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  • Withdrawn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
Vial Set
Generic name
General laboratory container, single-use
Model / Ref / Catalog
ASPP99DPTVL
Primary DI / UDI-DI
00886333220984
FDA product code
FMH
GMDN term
General laboratory container, single-use
Device class
Class I
Regulation number
864.3250
GUDID distribution status
In Commercial Distribution

Related devices

Category: General laboratory container, single-use

Similar devices

Other devices filed under FDA product code FMH (Container, Specimen, Sterile).

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)