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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
Frontal sinus file/rasp FDA UDI
Device Name
Integra® Jarit® Wiener Antrum Rasp, 7-3/4", Medium, 4mm Wide, Trocar Tip FDA UDI
Model / Reference
400235 FDA UDI
Description
Integra® Jarit® Wiener Antrum Rasp, 7-3/4", Medium, 4mm Wide, Trocar Tip FDA UDI

Identifiers

Catalog Number
400-235 FDA UDI
Primary DI / UDI-DI
10381780190967 FDA UDI
FDA Product Code
KAZ FDA UDI
GMDN Term
Frontal sinus file/rasp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Dimensions & Sizes

Size
Width — 4 Millimeter FDA UDI

Category: Frontal sinus file/rasp

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

Similar devices

Also classified as Frontal sinus file/rasp.

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 4a3429ff-2cf5-4d90-8a08-73cb9858a714 36 fields · synced Jun 9, 2026