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MicroFrance®

FDA UDI

Class I (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
MicroFrance® FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
MicroFrance® Bizeau self-retaining retractor, 160 mm length FDA UDI
Model / Reference
MCL37 FDA UDI
Description
MicroFrance® Bizeau self-retaining retractor, 160 mm length FDA UDI

Identifiers

Catalog Number
MCL37 FDA UDI
Primary DI / UDI-DI
10381780105596 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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: Rigid optical laryngopharyngoscope

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Similar devices

Also classified as Rigid optical laryngopharyngoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI 1380fd17-a0b3-4e60-9f97-913e711d7e97 35 fields · synced Jun 22, 2026