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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
General-purpose medical fibre padding FDA UDI
Device Name
PADDING,UNDERCAST,COTTON, 3X4YD STERILE FDA UDI
Model / Reference
DYNJ066003 FDA UDI
Description
PADDING,UNDERCAST,COTTON, 3X4YD STERILE FDA UDI

Identifiers

Catalog Number
DYNJ066003 FDA UDI
Primary DI / UDI-DI
10080196824779 FDA UDI
FDA Product Code
ITG FDA UDI
GMDN Term
General-purpose medical fibre padding FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

No

FDA UDI

Over-the-Counter

Yes

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: General-purpose medical fibre padding

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

Similar devices

Also classified as General-purpose medical fibre padding.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30ac4aa9-709e-4154-89c5-ae5f478444bb 35 fields · synced May 30, 2026