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Busse Hospital Disposables

FDA UDI

Class I (US FDA UDI)

by Robert Busse & Co., Inc.

Identity

Trade Name
Busse Hospital Disposables FDA UDI
Generic Name
Skin staple remover, single-use FDA UDI
Device Name
Skin Staple Remover FDA UDI
Model / Reference
716 FDA UDI
Description
Skin Staple Remover FDA UDI

Identifiers

Primary DI / UDI-DI
00849233010635 FDA UDI
FDA Product Code
HBS FDA UDI
GMDN Term
Skin staple remover, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4190 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: Skin staple remover, single-use

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

Similar devices

Also classified as Skin staple remover, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2bf8fceb-42f8-44d8-975e-6ff88220c43a 34 fields · synced Jun 1, 2026