Kilde Medic Biothesiometer X1
by Kilde & Co. ApS EUDAMED
Active
Ref 81000Model Kilde Medic Biothesiometer / Vibrometer / Sensiometer
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number5745000041KMBTMUP | Date21 Aug 2026 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
European Union — CE/MDR Active
Certificates
No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.
Specification
- Device Name
- Kilde Medic Biothesiometer / Vibrometer / Sensiometer
- Model / Reference
- Kilde Medic Biothesiometer / Vibrometer / Sensiometer, 81000
- Primary DI / UDI-DI
- 05745000042159
- Basic UDI-DI
- 5745000041KMBTMUP
- Direct Marketing DI
- 05745000042159
- EMDN Code
- Z12109004 Vibration threshold meters (vibrometer)
- Device Class
- Class I
- Market of Registration
- Denmark
Manufacturer details
- EUDAMED SRN
- DK-MF-000046232
From the manufacturer
Manufacturer's product page: KKildeMedic
Other devices from Kilde & Co. ApS
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No