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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-closure adhesive strip FDA UDI
Device Name
Butterfly Closures, all one size, 1 3/4 IN x 3/8 IN FDA UDI
Model / Reference
041520863461 FDA UDI
Description
Butterfly Closures, all one size, 1 3/4 IN x 3/8 IN FDA UDI

Identifiers

Primary DI / UDI-DI
00041520863461 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-closure adhesive strip 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

Yes

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-closure adhesive strip

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-closure adhesive strip.

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 985e31e7-707e-45d4-b400-f260fe3ad6b0 33 fields · synced Jun 8, 2026