← Back to catalogue

Integra® Jarit®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Jarit® FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
Integra® Jarit® Ruskin-Jay Rongeur, 8", 6mm Bite, Heavy, Light Curve FDA UDI
Model / Reference
230216 FDA UDI
Description
Integra® Jarit® Ruskin-Jay Rongeur, 8", 6mm Bite, Heavy, Light Curve FDA UDI

Identifiers

Catalog Number
230-216 FDA UDI
Primary DI / UDI-DI
10381780165477 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Orthopaedic joint/limb rongeur

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

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b5448c5e-32d5-4abf-855d-1d1098490db7 35 fields · synced Jun 9, 2026