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Integra® Jarit®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Jarit® FDA UDI
Generic Name
Suprapubic catheter introducer, reusable FDA UDI
Device Name
Integra® Jarit® O-Ring For #600-428, Package Of 6 FDA UDI
Model / Reference
6304262 FDA UDI
Description
Integra® Jarit® O-Ring For #600-428, Package Of 6 FDA UDI

Identifiers

Catalog Number
630-4262 FDA UDI
Primary DI / UDI-DI
10381780157236 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Suprapubic catheter introducer, 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suprapubic catheter introducer, reusable

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

Similar devices

Also classified as Suprapubic catheter introducer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra LifeSciences Production Corporation

Sources (1)

  • FDA UDI a725bc73-ba3b-4eb9-811d-3e989b3a6adc 35 fields · synced Jun 9, 2026