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Gill

FDA UDI

Class I (US FDA UDI)

by The Radebaugh-Fetzer Company

Identity

Trade Name
Gill FDA UDI
Generic Name
Bandage scissors, reusable FDA UDI
Device Name
Lister Bandage Scissors 5 1/2" FDA UDI
Model / Reference
883603 FDA UDI
Description
Lister Bandage Scissors 5 1/2" FDA UDI

Identifiers

Catalog Number
883603 FDA UDI
Primary DI / UDI-DI
00850047707307 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Bandage scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bandage scissors, reusable

Gill by The Radebaugh-Fetzer Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bandage scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b19741ac-c2f5-4ae1-843a-77f03b49f05a 35 fields · synced May 30, 2026