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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
Laparoscopic trocar blade, reusable FDA UDI
Device Name
Integra® MicroFrance® Sealing blue Cap for 5 mm trocar FDA UDI
Model / Reference
CEV105P6 FDA UDI
Description
Integra® MicroFrance® Sealing blue Cap for 5 mm trocar FDA UDI

Identifiers

Catalog Number
CEV105P6 FDA UDI
Primary DI / UDI-DI
10381780091561 FDA UDI
510(k) Number
K993653 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Laparoscopic trocar blade, 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: Laparoscopic trocar blade, reusable

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

Similar devices

Also classified as Laparoscopic trocar blade, reusable.

Cleared under the same submission

K993653 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Microfrance

Sources (1)

  • FDA UDI 00a7e546-9845-49dc-aef3-1f92ce2be2a5 37 fields · synced May 30, 2026