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Bone Marrow Tray BMT1000

by Argon Medical Devices, Inc.

Bone Marrow Tray BMT1000 is a Class II device made by Argon Medical Devices, Inc., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 00886333007851), 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 Number00886333007851 UDI-DI Date20 Sep 2016ListedStatusListed 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  • Withdrawn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
Bone Marrow Tray
Generic name
Bone marrow biopsy needle, single-use
Model / Ref / Catalog
BMT1000
Primary DI / UDI-DI
00886333007851
FDA product code
KNW
GMDN term
Bone marrow biopsy needle, single-use
Device class
Class II
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone marrow biopsy needle, single-use

Similar devices in this category

Other devices filed under Bone marrow biopsy needle, single-use.

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)