Integra® Jarit®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name: Integra® Jarit® FDA UDI
Generic Name: Laparoscopic access cannula, reusable FDA UDI
Device Name: Integra® Jarit® Reducer Sleeve, 7-1/2", For 12.5-5.5mm Trocars FDA UDI
Model / Reference: 600468 FDA UDI
Description: Integra® Jarit® Reducer Sleeve, 7-1/2", For 12.5-5.5mm Trocars FDA UDI

Identifiers

Catalog Number: 600-468 FDA UDI
Primary DI / UDI-DI: 10381780160953 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic access cannula, reusable

Integra® Jarit® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Laparoscopic access cannula, reusable.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Integra LifeSciences Production Corporation

Sources (1)

FDA UDI aab7c13b-6e38-43d3-a4b4-7125b534b4c4 35 fields · synced Jun 9, 2026