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CareOne

FDA UDI

Class I (US FDA UDI)

by Ahold U.S.A., Inc.

Identity

Trade Name
CareOne FDA UDI
Generic Name
Skin-cover adhesive strip, antimicrobial FDA UDI
Device Name
Extra Large Smart-Flex Adhesive Bandages Antibacterial, all one size, 2 3/4 in x 3 1/2 in FDA UDI
Model / Reference
041520143273 FDA UDI
Description
Extra Large Smart-Flex Adhesive Bandages Antibacterial, all one size, 2 3/4 in x 3 1/2 in FDA UDI

Identifiers

Catalog Number
04152014327 FDA UDI
Primary DI / UDI-DI
00041520143273 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-cover adhesive strip, antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-cover adhesive strip, antimicrobial

CareOne by Ahold U.S.A., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-cover adhesive strip, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ahold U.S.A., Inc.

Sources (1)

  • FDA UDI 264b16d1-195d-4cff-b209-70f80748baf4 34 fields · synced May 30, 2026