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Bone Marrow Tray

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Bone Marrow Tray FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
Bone Marrow Tray FDA UDI
Model / Reference
BMT1000 FDA UDI
Description
Bone Marrow Tray FDA UDI

Identifiers

Catalog Number
BMT1000 FDA UDI
Primary DI / UDI-DI
00886333007851 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Bone marrow biopsy needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone marrow biopsy needle, single-use

Bone Marrow Tray by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fdd1259a-6b50-4ffa-8cbf-cb7d6c91faaa 35 fields · synced Jun 9, 2026