← Back to catalogue

MicroFrance®

FDA UDI

Class II (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
MicroFrance® FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
MicroFrance® Curved scissors insert serrated blades 8mm insulated tube 3.5mm diam. 210mm length WL 230mm includes cleaning port CEV39L FDA UDI
Model / Reference
CEV893IU FDA UDI
Description
MicroFrance® Curved scissors insert serrated blades 8mm insulated tube 3.5mm diam. 210mm length WL 230mm includes cleaning port CEV39L FDA UDI

Identifiers

Catalog Number
CEV893IU FDA UDI
Primary DI / UDI-DI
10381780259671 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, 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: Rigid endoscopic tissue manipulation forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI 60ab2d17-0587-4f16-a351-a020e3b83f2a 36 fields · synced Jun 1, 2026