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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
Lumbar puncture kit FDA UDI
Device Name
Safety-Deluxe Lumbar Puncture Tray with 20G x 3.5" Spinal Needle & Manometer FDA UDI
Model / Reference
974B FDA UDI
Description
Safety-Deluxe Lumbar Puncture Tray with 20G x 3.5" Spinal Needle & Manometer FDA UDI

Identifiers

Primary DI / UDI-DI
00849233008779 FDA UDI
FDA Product Code
FMJ FDA UDI
GMDN Term
Lumbar puncture kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2500 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

No

FDA UDI

Category: Lumbar puncture 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 Lumbar puncture kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Robert Busse & Co., Inc.

Sources (1)

  • FDA UDI 70197508-805b-4241-ad61-0094844c284d 34 fields · synced May 30, 2026