Identity
- Trade Name
- Up & Up FDA UDI
- Generic Name
- Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- A convenience kit consisting of 7 up&up One Step Ovulation Predictor Tests + 1 up&up Early Result Pregnancy Test FDA UDI
- Model / Reference
- One Step Ovulation Predictor PLUS Early Result Pregnancy Test FDA UDI
- Description
- A convenience kit consisting of 7 up&up One Step Ovulation Predictor Tests + 1 up&up Early Result Pregnancy Test FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00492450308636 FDA UDI
- FDA Product Code
- LCX FDA UDICEP FDA UDI
- GMDN Term
- Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1155 FDA UDI862.1485 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Up & Up by Target Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Target Corporation
Sources (1)
- FDA UDI 52c8b7ff-53b6-4cc5-91ec-3f90c3d97276 36 fields · synced Jun 1, 2026