Identity
- Trade Name
- CVS Health FDA UDI
- Generic Name
- Natural conception assistance kit FDA UDI
- Device Name
- CVS Health Digital Ovulation Test Kit 10 ct FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- CVS Health Digital Ovulation Test Kit 10 ct FDA UDI
Identifiers
- Catalog Number
- 322548 FDA UDI
- Primary DI / UDI-DI
- 00050428083581 FDA UDI
- FDA Product Code
- NGE FDA UDI
- GMDN Term
- Natural conception assistance kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1485 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Natural conception assistance kit
CVS Health by Woonsocket Prescription Center, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Medichoice — OWENS & MINOR DISTRIBUTION, INC. · Class II
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
- Woonsocket Prescription Center, Incorporated
Sources (1)
- FDA UDI 0402f282-961b-4ec0-9ce8-81919e3ae614 35 fields · synced Jun 1, 2026