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: Assorted Waterproof Clear Bandages Antibacterial, 1 IN x 2 1/2 IN (25 mm x 63 mm); 3/4 IN x 2 IN (19 mm x 50 mm); 3/4 IN x 1 1/2 IN (19 mm x 38 mm) FDA UDI
Model / Reference: 041520078223 FDA UDI
Description: Assorted Waterproof Clear Bandages Antibacterial, 1 IN x 2 1/2 IN (25 mm x 63 mm); 3/4 IN x 2 IN (19 mm x 50 mm); 3/4 IN x 1 1/2 IN (19 mm x 38 mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00041520078223 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ahold U.S.A., Inc.

Sources (1)

FDA UDI 8d2a6705-d2b6-467e-95ba-dc3b3ef8a0e7 33 fields · synced Jun 8, 2026