← Back to catalogue

MicroFrance®

FDA UDI

Class I (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
MicroFrance® FDA UDI
Generic Name
Tongue depressor, surgical FDA UDI
Device Name
TONGUE DEPRESSOR MCL206A4 40X85MM MORI FDA UDI
Model / Reference
MCL206A4 FDA UDI
Description
TONGUE DEPRESSOR MCL206A4 40X85MM MORI FDA UDI

Identifiers

Catalog Number
MCL206A4 FDA UDI
Primary DI / UDI-DI
10381780105268 FDA UDI
FDA Product Code
KBL FDA UDI
GMDN Term
Tongue depressor, surgical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Tongue depressor, surgical

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

Similar devices

Also classified as Tongue depressor, surgical.

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 16693672-9405-4983-9930-5fff5da51ddb 35 fields · synced May 31, 2026