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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
General-purpose curette FDA UDI
Device Name
G-98-A Nail Curette 1.5mm/2.5mm 5 1/2" Double-Ended 1/3 FDA UDI
Model / Reference
883263 FDA UDI
Description
G-98-A Nail Curette 1.5mm/2.5mm 5 1/2" Double-Ended 1/3 FDA UDI

Identifiers

Catalog Number
883263 FDA UDI
Primary DI / UDI-DI
00850047707284 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
General-purpose curette 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: General-purpose curette

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

Similar devices

Also classified as General-purpose curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3518b543-5df7-4f34-923e-79f19b83f236 35 fields · synced May 30, 2026