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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
Laryngeal injection kit FDA UDI
Device Name
Integra® MicroFrance® Injection pistol with needle MCL55-1 FDA UDI
Model / Reference
MCL55 FDA UDI
Description
Integra® MicroFrance® Injection pistol with needle MCL55-1 FDA UDI

Identifiers

Catalog Number
MCL55 FDA UDI
Primary DI / UDI-DI
10381780105794 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Laryngeal injection kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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: Laryngeal injection kit

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

Similar devices

Also classified as Laryngeal injection kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI 78eba502-db61-4078-be64-ff53bf477ae6 36 fields · synced Jun 8, 2026