← Back to catalogue

Integra®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® FDA UDI
Generic Name
Paranasal sinus curette FDA UDI
Device Name
Integra® Frontal Sinus Recess Curette, Straight FDA UDI
Model / Reference
3714703 FDA UDI
Description
Integra® Frontal Sinus Recess Curette, Straight FDA UDI

Identifiers

Catalog Number
3714703 FDA UDI
Primary DI / UDI-DI
10381780080671 FDA UDI
FDA Product Code
KAP FDA UDI
GMDN Term
Paranasal sinus curette 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Paranasal sinus curette

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

Similar devices

Also classified as Paranasal sinus curette.

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 150bfb31-75f6-4e9b-9253-e17df2e2ee12 35 fields · synced Jun 9, 2026