Beehive
by Aksdent Global Dental Ve Tibbi̇ Ci̇hazlar San. Ti̇c. Ltd. Şti̇ 10 variants
Ref P-219Model C-002
Active
CE MDR
Valid until
18 Dec 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8682615911AHSHCN 08682615911234 | Date17 Jan 2025 | StatusActive |
Certificates
- 0425-MDR-030110-00 Active
Quality management system EU MDR
- Certifier
- ICIM S.P.A. 0425
- Issued
- 19 Dec 2024
- Expires
- 18 Dec 2029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Dental High-Speed FO Handpiece
- Model / Reference
- C-002, P-219
- Primary DI / UDI-DI
- 08682615911234
- Basic UDI-DI
- 8682615911AHSHCN
- EMDN Code
- Z12110102 Dental drills
- Device Class
- Class IIa
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000039281
Other devices from Aksdent Global Dental Ve Tibbi̇ Ci̇hazlar San. Ti̇c. Ltd. Şti̇
See all devices from Aksdent Global Dental Ve Tibbi̇ Ci̇hazlar San. Ti̇c. Ltd. Şti̇ →
Properties
Other properties (13)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No