← Back to catalogue

Integra® Jarit®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Jarit® FDA UDI
Generic Name
Cranial bur, reusable FDA UDI
Device Name
Integra® Jarit® McKenzie Enlarging Burr FDA UDI
Model / Reference
295150 FDA UDI
Description
Integra® Jarit® McKenzie Enlarging Burr FDA UDI

Identifiers

Catalog Number
295-150 FDA UDI
Primary DI / UDI-DI
10381780157632 FDA UDI
FDA Product Code
HBG FDA UDI
GMDN Term
Cranial bur, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4300 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: Cranial bur, 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 Cranial bur, reusable.

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

Manufacturer
Integra LifeSciences Production Corporation

Sources (1)

  • FDA UDI 42d8f41b-ebcf-492b-805c-aa422bb764ed 35 fields · synced Jun 9, 2026