thermometer
by K-jump Health Co., Ltd. Taiwan EUDAMED510(k)
Ref KD&KI510(k) K060240
Product code FLLEMDN V0301010299
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-471094497KD&KI8N | Date23 Feb 2022 | StatusActive |
| United States | FDA 510(k)SESE 510(k) | NumberK060240 | Date19 May 2006 | StatusActive |
Coverage
- Active
- Expiring (legacy directive)
- Not covered
- United States
- European Union
Specification
- Device Name
- thermometer
- Model / Reference
- KD&KI
- Primary DI / UDI-DI
- D-471094497KD&KI8N
- Basic UDI-DI
- B-471094497KD&KI8N
- 510(k) Number
- FDA Product Code
- FLL
- EMDN Code
- V0301010299 Digital thermometers - other
- Device Class
- Class IIa EUDAMEDClass II 510(k)
- Regulation
- 21 CFR Part 880.2910
- Market of Registration
- Germany
- Advisory Committee
- General Hospital
- FDA Decision
- SESE Substantially Equivalent
Truth per registry
| Field | EUDAMED | 510(k) |
|---|---|---|
| Device Class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- TW-MF-000020665
- Authorised representative
- Polygreen Germany GmbH DE-AR-000019484
Other devices from K-jump Health Co., Ltd.
Properties & raw data
Show properties, registry sources and raw records
Other properties (10)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Incorporates Medicinal Product: No
Sources (2)
- EUDAMED f1f775dc-e82c-41cd-ad78-19b598d2e6c3
- FDA 510(k) K060240