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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
ENT speculum holder FDA UDI
Device Name
Integra® MicroFrance® Operating table clamp for CEV980A CEV980B CEV990 MCO978 and MCO980 FDA UDI
Model / Reference
CEV984 FDA UDI
Description
Integra® MicroFrance® Operating table clamp for CEV980A CEV980B CEV990 MCO978 and MCO980 FDA UDI

Identifiers

Catalog Number
CEV984 FDA UDI
Primary DI / UDI-DI
10381780097440 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
ENT speculum holder 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

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: ENT speculum holder

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

Similar devices

Also classified as ENT speculum holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI c249ca1c-02c5-4488-8508-8190fb5fb2d3 36 fields · synced May 30, 2026