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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
Low-resistance epidural syringe FDA UDI
Device Name
10ml Plastic Loss of Resistance (LOR) Syringe with luer slip tip FDA UDI
Model / Reference
596 FDA UDI
Description
10ml Plastic Loss of Resistance (LOR) Syringe with luer slip tip FDA UDI

Identifiers

Catalog Number
596 FDA UDI
Primary DI / UDI-DI
00849233010482 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Low-resistance epidural syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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: Low-resistance epidural syringe

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 Low-resistance epidural syringe.

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 784b9c1e-1b71-442b-8ae8-35a20405955a 35 fields · synced May 29, 2026