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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
Basic electric toothbrush FDA UDI
Device Name
Power Toothbrush, Dual Zone Advanced Clean, Soft FDA UDI
Model / Reference
STT FDA UDI
Description
Power Toothbrush, Dual Zone Advanced Clean, Soft FDA UDI

Identifiers

Primary DI / UDI-DI
00041520125378 FDA UDI
FDA Product Code
JEQ FDA UDI
GMDN Term
Basic electric toothbrush FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6865 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic electric toothbrush

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

Similar devices

Also classified as Basic electric toothbrush.

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 90c1fd49-c676-4d18-9820-d383bf46ec3a 33 fields · synced Jun 8, 2026