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Integra® MicroFrance®

FDA UDI

Class II (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
Integra® MicroFrance® FDA UDI
Generic Name
Surgical irrigation/aspiration handpiece, reusable FDA UDI
Device Name
Integra® MicroFrance® Gayet handle for suction tubes 3.5 and 5 mm diameter FDA UDI
Model / Reference
CEV103BG FDA UDI
Description
Integra® MicroFrance® Gayet handle for suction tubes 3.5 and 5 mm diameter FDA UDI

Identifiers

Catalog Number
CEV103BG FDA UDI
Primary DI / UDI-DI
10381780091455 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical irrigation/aspiration handpiece, 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical irrigation/aspiration handpiece, reusable

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

Similar devices

Also classified as Surgical irrigation/aspiration handpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI b5b438fc-a2db-4e79-a730-2730a6682ae5 36 fields · synced Jun 7, 2026