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MicroFrance®

FDA UDI

Class I (US FDA UDI)

by Integra Microfrance

Identity

Trade Name
MicroFrance® FDA UDI
Generic Name
Ear knife FDA UDI
Device Name
LANCET 7725P2 3PK 80MM N2 FDA UDI
Model / Reference
7725P2 FDA UDI
Description
LANCET 7725P2 3PK 80MM N2 FDA UDI

Identifiers

Catalog Number
7725P2 FDA UDI
Primary DI / UDI-DI
10381780088547 FDA UDI
FDA Product Code
JYO FDA UDI
GMDN Term
Ear knife 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: Ear knife

MicroFrance is a high-quality, one-piece hand-held manual surgical instrument designed for ear dissection and cutting. It features a sharp, single-edged cutting blade, made from high-grade stainless steel, and has a long slender shaft with a handle at the proximal end. MicroFrance is intended for use in conjunction with other medical devices, particularly in procedures involving ear anatomy.

Similar devices

Also classified as Ear knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI 361c329d-7634-456d-9165-a1bb3fcd670f 35 fields · synced Jun 27, 2026