← Back to catalogue

Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Woven gauze roll/sheet FDA UDI
Device Name
BANDAGE,GAUZE,BULKEE II,4.5"X4.1YD,NS,LF FDA UDI
Model / Reference
NON25855P FDA UDI
Description
BANDAGE,GAUZE,BULKEE II,4.5"X4.1YD,NS,LF FDA UDI

Identifiers

Catalog Number
NON25855P FDA UDI
Primary DI / UDI-DI
20080196746030 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze roll/sheet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Woven gauze roll/sheet

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

Similar devices

Also classified as Woven gauze roll/sheet.

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

Sources (1)

  • FDA UDI b35e138f-95ec-4e02-9d94-6afe599a8fe1 35 fields · synced May 30, 2026