Integra® MicroFrance®

FDA UDI

Class II (US FDA UDI)

by Integra Microfrance

Identity

Trade Name: Integra® MicroFrance® FDA UDI
Generic Name: Suturing needle holder, reusable FDA UDI
Device Name: Integra® MicroFrance® Needle holder with tungsten carbide curved jaws, 5 mm diameter, 335 mm length, ergonomic handle FDA UDI
Model / Reference: CEV738T5 FDA UDI
Description: Integra® MicroFrance® Needle holder with tungsten carbide curved jaws, 5 mm diameter, 335 mm length, ergonomic handle FDA UDI

Identifiers

Catalog Number: CEV738T5 FDA UDI
Primary DI / UDI-DI: 10381780095378 FDA UDI
FDA Product Code: HET FDA UDI
GMDN Term: Suturing needle holder, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.1720 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: Suturing needle holder, reusable

Integra® 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 c419b4b2-85ac-4a06-a536-0bb6aaa5237f 36 fields · synced May 30, 2026