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Curity

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Curity FDA UDI
Generic Name
Gauze strip, antimicrobial FDA UDI
Device Name
Plain Packing Strip FDA UDI
Model / Reference
7632 FDA UDI
Description
Plain Packing Strip FDA UDI

Identifiers

Catalog Number
7632 FDA UDI
Primary DI / UDI-DI
30884521068678 FDA UDI
FDA Product Code
GDY FDA UDI
GMDN Term
Gauze strip, antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4450 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 0.50 Inch FDA UDI
Length — 15 Feet FDA UDI

Category: Gauze strip, antimicrobial

Curity by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gauze strip, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI cbc4a263-e03f-4b6d-afae-67539b5f98b3 37 fields · synced May 31, 2026