Identity
- Trade Name
- CareOne FDA UDI
- Generic Name
- Adhesive bandage FDA UDI
- Device Name
- Watershield Adhesive Pads, all one size, 3 IN x 4 IN FDA UDI
- Model / Reference
- 041520010681 FDA UDI
- Description
- Watershield Adhesive Pads, all one size, 3 IN x 4 IN FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00041520010681 FDA UDI
- FDA Product Code
- KGX FDA UDI
- GMDN Term
- Adhesive bandage 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: Adhesive bandageSkin-cover adhesive strip, non-antimicrobial
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-cover adhesive strip, non-antimicrobial.
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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 0fbe449e-a2a3-4338-88c6-4faa96f407ae 33 fields · synced Jun 8, 2026