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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Adenoid curette, single-use FDA UDI
Device Name
14-23004 ADENOID CURETTE BLUE SIZE 4 FDA UDI
Model / Reference
1423004R FDA UDI
Description
14-23004 ADENOID CURETTE BLUE SIZE 4 FDA UDI

Identifiers

Catalog Number
1423004R FDA UDI
Primary DI / UDI-DI
10888277377592 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

Yes

FDA UDI

Single Use

Yes

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

Category: Adenoid curette, single-use

Medline by Medline Industries, Inc. — 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
Medline Industries, Inc.

Sources (1)

  • FDA UDI 17e3b2ea-e85d-48eb-8fd7-cdf2565763a0 35 fields · synced May 30, 2026