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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Non-woven gauze pad, non-sterile FDA UDI
Device Name
GAUZE, SPONGE, IV, 2"X2", 6PLY, ST, 2'S FDA UDI
Model / Reference
NON256001 FDA UDI
Description
GAUZE, SPONGE, IV, 2"X2", 6PLY, ST, 2'S FDA UDI

Identifiers

Catalog Number
NON256001 FDA UDI
Primary DI / UDI-DI
20080196692719 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-woven gauze pad, non-sterile 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

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: Non-woven gauze pad, non-sterile

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

Similar devices

Also classified as Non-woven gauze pad, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4be4c302-ef25-4ea4-a8f9-75c9f790b687 35 fields · synced May 31, 2026