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Busse Hospital Disposables

FDA UDI

Class II (US FDA UDI)

by Robert Busse & Co., Inc.

Identity

Trade Name
Busse Hospital Disposables FDA UDI
Generic Name
Bone marrow biopsy procedure kit FDA UDI
Device Name
Sterile Bone Marrow Biopsy / Aspiration Tray w/ Biopsy Needles & Aspiration Needle FDA UDI
Model / Reference
654 FDA UDI
Description
Sterile Bone Marrow Biopsy / Aspiration Tray w/ Biopsy Needles & Aspiration Needle FDA UDI

Identifiers

Catalog Number
654 FDA UDI
Primary DI / UDI-DI
00849233013285 FDA UDI
FDA Product Code
PRV FDA UDI
GMDN Term
Bone marrow biopsy procedure kit 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone marrow biopsy procedure kit

Busse Hospital Disposables by Robert Busse & Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy procedure kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 567d4e47-1da8-470a-a5f8-02db6123495b 36 fields · synced May 30, 2026