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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
Suturing needle holder, reusable FDA UDI
Device Name
Integra® Jarit® Microsurgery Needle Holder, 7", 0.9mm Tip, Jarit Stardust®, Round Handle, With Catch, Curved FDA UDI
Model / Reference
278117 FDA UDI
Description
Integra® Jarit® Microsurgery Needle Holder, 7", 0.9mm Tip, Jarit Stardust®, Round Handle, With Catch, Curved FDA UDI

Identifiers

Catalog Number
278-117 FDA UDI
Primary DI / UDI-DI
10381780186663 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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: Suturing needle holder, reusable

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

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f42b645e-20bd-4779-a416-9d99723200b3 35 fields · synced Jun 9, 2026