← 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
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Integra® Jarit® Mills Coronary Mammary Forceps, 7", Tissue, Ring Tip, 0.5mm Inside Diameter, 1mm Outside Diameter FDA UDI
Model / Reference
310528 FDA UDI
Description
Integra® Jarit® Mills Coronary Mammary Forceps, 7", Tissue, Ring Tip, 0.5mm Inside Diameter, 1mm Outside Diameter FDA UDI

Identifiers

Catalog Number
310-528 FDA UDI
Primary DI / UDI-DI
10381780191834 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, 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: Surgical soft-tissue manipulation forceps, tweezers-like, 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 Surgical soft-tissue manipulation forceps, tweezers-like, 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

Sources (1)

  • FDA UDI ac4280ec-03f2-4995-9e9c-5734d3831801 35 fields · synced Jun 9, 2026