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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
General-purpose endoscopic needle, reusable FDA UDI
Device Name
Integra® MicroFrance® Needle with luer lock, 5 mm diameter, 300 mm length FDA UDI
Model / Reference
CEV65 FDA UDI
Description
Integra® MicroFrance® Needle with luer lock, 5 mm diameter, 300 mm length FDA UDI

Identifiers

Catalog Number
CEV65 FDA UDI
Primary DI / UDI-DI
10381780094975 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
General-purpose endoscopic needle, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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: General-purpose endoscopic needle, reusable

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

Similar devices

Also classified as General-purpose endoscopic needle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI bb3aa54c-fe0b-4fa6-950b-f7a71a2c4039 36 fields · synced May 30, 2026