Identity
- Trade Name
- Up & Up FDA UDI
- Generic Name
- Intermittent electronic patient thermometer FDA UDI
- Device Name
- Up&Up Automatic Digital BP Monitor, Wide-Range Cuff FDA UDI
- Model / Reference
- 094-01-0230 FDA UDI
- Description
- Up&Up Automatic Digital BP Monitor, Wide-Range Cuff FDA UDI
Identifiers
- Catalog Number
- 48-554 FDA UDI
- Primary DI / UDI-DI
- 00845717009324 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Intermittent electronic patient thermometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 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
Yes
FDA UDI
Convenience Kit
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Intermittent electronic patient thermometer
Up & Up by Target Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Target Corporation
Sources (1)
- FDA UDI cc29a252-ac40-4f19-876f-b8bd1ba650a1 34 fields · synced May 30, 2026