MicroFrance®

FDA UDI

Class II (US FDA UDI)

by Integra Microfrance

Identity

Trade Name: MicroFrance® FDA UDI
Generic Name: General-purpose surgical scissors, reusable FDA UDI
Device Name: MicroFrance® CORBINEAU CURVED SCISSORS, TITANIUM LARGE CURVED BLADES, 5 MM DIAMETER, 230 MM LENGTH, MICRO HANDLE FDA UDI
Model / Reference: CEC8605GT FDA UDI
Description: MicroFrance® CORBINEAU CURVED SCISSORS, TITANIUM LARGE CURVED BLADES, 5 MM DIAMETER, 230 MM LENGTH, MICRO HANDLE FDA UDI

Identifiers

Catalog Number: CEC8605GT FDA UDI
Primary DI / UDI-DI: 10381780091110 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose surgical scissors, reusable

MicroFrance® by Integra Microfrance — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Integra Microfrance

Sources (1)

FDA UDI b8f0cbd5-18bd-40f0-b0d8-03fd4ad10729 36 fields · synced May 30, 2026