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Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Curad FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Device Name
DBD-ELASTIC NET,SZ 1/2,STRETCH,4"X25YD,L FDA UDI
Model / Reference
NONNET012-1 FDA UDI
Description
DBD-ELASTIC NET,SZ 1/2,STRETCH,4"X25YD,L FDA UDI

Identifiers

Catalog Number
NONNET012-1 FDA UDI
Primary DI / UDI-DI
00080196341293 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, single-use 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

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: Skin treatment/dressing-supportive limb/finger bandage, single-use

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

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, 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 af249438-1ba6-444a-b79f-39cfc5511fea 35 fields · synced May 31, 2026