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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
Nasal breathing aid, external FDA UDI
Device Name
Drug Free Nasal Strips Extra Strength Tan FDA UDI
Model / Reference
041520125057 FDA UDI
Description
Drug Free Nasal Strips Extra Strength Tan FDA UDI

Identifiers

Primary DI / UDI-DI
00041520125057 FDA UDI
FDA Product Code
LWF FDA UDI
GMDN Term
Nasal breathing aid, external FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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: Nasal breathing aid, external

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

Similar devices

Also classified as Nasal breathing aid, external.

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 9a31c344-6d19-49cc-963c-b6f7e0d60210 33 fields · synced Jun 8, 2026