MicroFrance®

FDA UDI

Class I (US FDA UDI)

by Integra Microfrance

Identity

Trade Name: MicroFrance® FDA UDI
Generic Name: Flexible endoscopic biopsy forceps, reusable FDA UDI
Device Name: MicroFrance® Cupward forceps, upward opening 3.5 x 10 mm jaws, 600 mm length FDA UDI
Model / Reference: 7844T6L60 FDA UDI
Description: MicroFrance® Cupward forceps, upward opening 3.5 x 10 mm jaws, 600 mm length FDA UDI

Identifiers

Catalog Number: 7844T6L60 FDA UDI
Primary DI / UDI-DI: 10381780090335 FDA UDI
FDA Product Code: GEN FDA UDI
GMDN Term: Flexible endoscopic biopsy forceps, reusable 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

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

Yes

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: Flexible endoscopic biopsy forceps, reusable

MicroFrance® by Integra Microfrance — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Integra Microfrance

Sources (1)

FDA UDI 3d83f08e-e78c-4107-b619-b2494e92ddf5 35 fields · synced May 31, 2026