← Back to catalogue

Curad

FDA UDI

Class U (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
CURAD FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Device Name
GEL,GERM SHIELD,CURAD,0.5 OZ TUBE FDA UDI
Model / Reference
CUR45955GS FDA UDI
Description
GEL,GERM SHIELD,CURAD,0.5 OZ TUBE FDA UDI

Identifiers

Catalog Number
CUR45955GS FDA UDI
Primary DI / UDI-DI
00197344151878 FDA UDI
510(k) Number
K070333 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound hydrogel dressing, antimicrobial

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

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

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 63d6bc6d-834a-47e5-9a35-bc7b5952c61d 36 fields · synced Jun 8, 2026