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Curity

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Curity FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Non-adherent Strips,Oil Emulsion FDA UDI
Model / Reference
6115 FDA UDI
Description
Non-adherent Strips,Oil Emulsion FDA UDI

Identifiers

Catalog Number
6115 FDA UDI
Primary DI / UDI-DI
10884521068636 FDA UDI
FDA Product Code
KMF FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 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

No

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
Length — 8 Inch FDA UDI
Width — 3 Inch FDA UDI

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

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

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 90389b84-6090-4e30-b495-fd614fd1f224 37 fields · synced Jun 6, 2026