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MicroFrance®

FDA UDI

Class I (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
MicroFrance® FDA UDI
Generic Name
Tonsil snare FDA UDI
Device Name
LOOP 7754-3 20PK PRESHAPED LERMOYER FDA UDI
Model / Reference
7754-3 FDA UDI
Description
LOOP 7754-3 20PK PRESHAPED LERMOYER FDA UDI

Identifiers

Catalog Number
7754-3 FDA UDI
Primary DI / UDI-DI
10381780088707 FDA UDI
FDA Product Code
JYQ FDA UDI
GMDN Term
Tonsil snare 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: Tonsil snare

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

Similar devices

Also classified as Tonsil snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI a2b491f7-1171-4f3f-8a9b-af777d8f7212 35 fields · synced Jun 8, 2026