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Integra®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® FDA UDI
Generic Name
Adenoid curette, single-use FDA UDI
Device Name
Integra® Stubbs Adenoid Curette, 8-3/4", Size 0, 11mm Cutting Edge FDA UDI
Model / Reference
3734131 FDA UDI
Description
Integra® Stubbs Adenoid Curette, 8-3/4", Size 0, 11mm Cutting Edge FDA UDI

Identifiers

Catalog Number
3734131 FDA UDI
Primary DI / UDI-DI
10381780086338 FDA UDI
FDA Product Code
KBJ FDA UDI
GMDN Term
Adenoid curette, single-use 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

Dimensions & Sizes

Size
Width — 11 Millimeter FDA UDI

Category: Adenoid curette, single-use

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

Similar devices

Also classified as Adenoid curette, single-use.

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 b9b19f32-6fc5-42b4-b6dc-5eb28832d8eb 36 fields · synced Jun 9, 2026