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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Cotton wool ball FDA UDI
Device Name
MOHS CLOSURE FDA UDI
Model / Reference
DYNDA1370 FDA UDI
Description
MOHS CLOSURE FDA UDI

Identifiers

Catalog Number
DYNDA1370 FDA UDI
Primary DI / UDI-DI
10653160382928 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Cotton wool ball FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cotton wool ball

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cotton wool ball.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 725582ec-a461-438f-9402-9138e6fa5168 35 fields · synced Jun 6, 2026