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Integra® Jarit®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Jarit® FDA UDI
Generic Name
Open-surgery stone-retrieval forceps FDA UDI
Device Name
Integra® Jarit® Randall Kidney Stone Forceps, 7-3/4", Three Quarter Curve FDA UDI
Model / Reference
475472 FDA UDI
Description
Integra® Jarit® Randall Kidney Stone Forceps, 7-3/4", Three Quarter Curve FDA UDI

Identifiers

Catalog Number
475-472 FDA UDI
Primary DI / UDI-DI
10381780201700 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Open-surgery stone-retrieval forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery stone-retrieval forceps

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

Similar devices

Also classified as Open-surgery stone-retrieval forceps.

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 016d1f30-b8f3-4229-ab10-b2aad449f016 35 fields · synced Jun 9, 2026