raiing iThermonitor WT701
by Raiing Medical Company 2 variants
raiing iThermonitor WT701 is a Class II device made by Raiing Medical Company, cleared under FDA 510(k) K132761 on 8 Jul 2014 and listed in FDA GUDID since 1 Nov 2019 (UDI-DI 06957324200286), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06957324200286 | Date1 Nov 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK132761 | Date8 Jul 2014 | StatusActive |
Official records
- AccessGUDID record 06957324200286
- FDA 510(k) database K132761
Across registries
- FDA 510(k) K132761 decided 8 Jul 2014 Active
- FDA GUDID UDI-DI 06957324200286 listed 1 Nov 2019 Listed
Timeline
- Cleared FDA 510(k) K132761
- Listed FDA GUDID 06957324200286
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- raiing iThermonitor
- Generic name
- Continuous electronic patient thermometer, battery-powered
- Model / reference
- WT701
- Primary DI / UDI-DI
- 06957324200286
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Continuous electronic patient thermometer, battery-powered
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Liquid Chemical
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