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Sign in to claim this brandAhold U.S.A., Inc.
US
Last updated May 30, 2026
What Ahold U.S.A., Inc. makes
The company manufactures unscented menstrual pads and tampons, dental floss, non-woven gauze pads, basic electric toothbrushes, and skin-cover adhesive strips—both antimicrobial and non-antimicrobial varieties. It also produces autoinjector needles designed for use with prefilled pens.
These products are classified under FDA’s Class I and Class II regulations, with some falling under the exempt (N) or unclassified (U) categories. They are listed in the FDA’s Unique Device Identifier (UDI) database, and the company operates in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Ahold U.S.A., Inc. manufacture?
Ahold U.S.A., Inc. produces a range of medical devices primarily focused on personal hygiene and minor wound care. These include unscented menstrual pads and tampons, dental floss, non-woven gauze pads, basic electric toothbrushes, and skin-cover adhesive strips—both antimicrobial and non-antimicrobial. Additionally, they manufacture autoinjector needles designed for use with prefilled pens, which are commonly used in diabetes management.
Where is Ahold U.S.A., Inc. based, and what does this mean for its devices?
Ahold U.S.A., Inc. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations, including classification under FDA’s device categories (Class I, Class II, exempt (N), or unclassified (U)) and mandatory listing in the FDA’s Unique Device Identifier (UDI) database. This ensures compliance with U.S. medical device standards.
Which regulatory registries or databases list Ahold U.S.A., Inc.’s devices?
Ahold U.S.A., Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their distribution and use, ensuring transparency and traceability for regulatory and clinical purposes. This listing is required for devices classified under FDA regulations.
How are Ahold U.S.A., Inc.’s devices classified by the FDA?
Ahold U.S.A., Inc.’s devices fall under FDA’s Class I and Class II classifications, which determine the regulatory controls applied to them. Class I devices generally pose minimal risk and may have fewer regulatory requirements, while Class II devices require stricter controls due to moderate risk. Some of their devices are classified as exempt (N) or unclassified (U), meaning they either have no specific regulatory requirements or are not yet assigned a formal class. Classification depends on factors like intended use and potential risk.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- premier-brands.com
- —
- —
- [email protected]
- Phone
- (718)878-3097
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 170199058
Catalogue (177)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Care One | 600790 | FDA UDI | Class I | Active |
| Ahold - CareOne UPP 12mm pen needles | AN 3829AH | FDA UDI | Class II | Active |
| Care One | 278675 | FDA UDI | Class I | Active |
| Care One | Sterile Multi-Purpose Solution | FDA UDI | Class II | Active |
| Care One | 680450 | FDA UDI | Class I | Active |
| CareOne | UQW | FDA UDI | Class I | Active |
| CareOne | 041520143273 | FDA UDI | Class I | Active |
| CareOne | 041520078261 | FDA UDI | Class I | Active |
| CareOne | UGN | FDA UDI | Class I | Active |
| CareOne | 041520143280 | FDA UDI | Class I | Active |
| Ahold - CareOne UPP 5mm pen needles | AN 3850AH | FDA UDI | Class II | Active |
| CareOne | SRC | FDA UDI | Class I | Active |
| CareOne | 041520877642 | FDA UDI | Class I | Active |
| Care One | 663290 | FDA UDI | Class I | Active |
| CareOne | 041520096777 | FDA UDI | Class I | Active |
| CareOne Tampons | CA31812UO/1 | FDA UDI | Class II | Active |
| CareOne | VKG | FDA UDI | Class I | Active |
| CareOne | 041520871350 | FDA UDI | Class I | Active |
| Care One | 054793 | FDA UDI | Class II | Active |
| CareOne | 041520882035 | FDA UDI | Class I | Active |
| CareOne | 041520078193 | FDA UDI | Class I | Active |
| CareOne | UVH | FDA UDI | Class I | Active |
| Care One | AN 3860AH | FDA UDI | Class II | Active |
| Care One | 667870 | FDA UDI | Class I | Active |
| CareOne | 041520863393 | FDA UDI | Class I | Active |
| CareOne | 041520863423 | FDA UDI | Class I | Active |
| Care One | Multi-Purpose Solution (For Soft Contact Lenses) | FDA UDI | Class II | Active |
| CareOne | 041520125026 | FDA UDI | Class I | Unknown |
| CareOne Tampons | CA12012F/2 | FDA UDI | Class II | Active |
| CareOne Tampons | CA34012FN/2 | FDA UDI | Class II | Active |
| Care One | AT 0270AH | FDA UDI | Class II | Active |
| Care One | 278676 | FDA UDI | Class I | Active |
| CareOne | 79002 | FDA UDI | U | Active |
| CareOne | 041520863317 | FDA UDI | Class I | Active |
| CareOne | 041520125040 | FDA UDI | Class I | Active |
| CareOne | 041520019714 | FDA UDI | Class I | Active |
| CareOne | 041520126634 | FDA UDI | N | Active |
| CareOne | 041520863300 | FDA UDI | Class I | Active |
| Care One | Early Result Pregnancy Test | FDA UDI | Class II | Active |
| CareOne | 041520089410 | FDA UDI | Class I | Active |
| CareOne | UVH | FDA UDI | Class I | Active |
| Care One | 67-541K | FDA UDI | Class II | Active |
| CareOne | 041520875754 | FDA UDI | Class I | Active |
| CareOne Tampons | CA24012FN/2 | FDA UDI | Class II | Active |
| Care One | 490180 | FDA UDI | Class I | Active |
| CareOne | TLK | FDA UDI | Class I | Active |
| Care One | 532164 | FDA UDI | U | Active |
| CareOne | 041520078230 | FDA UDI | Class I | Active |
| CareOne | 041520096784 | FDA UDI | Class I | Active |
| Care One | 489770 | FDA UDI | Class I | Active |
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