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MicroFrance®

FDA UDI

Class I (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
MicroFrance® FDA UDI
Generic Name
Frontal sinus file/rasp FDA UDI
Device Name
FORCEPS 7762-5 STR W/SUCT KLOSSEK CUP FDA UDI
Model / Reference
7762-5 FDA UDI
Description
FORCEPS 7762-5 STR W/SUCT KLOSSEK CUP FDA UDI

Identifiers

Catalog Number
7762-5 FDA UDI
Primary DI / UDI-DI
10381780538516 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Frontal sinus file/rasp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Frontal sinus file/rasp

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

Similar devices

Also classified as Frontal sinus file/rasp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI b7e9f1b9-2a69-4abc-a2be-9b7f995565e9 35 fields · synced Jun 8, 2026