Planning Dual Abutment
by Dentium Co., Ltd. 15 variants
Ref PDAB4515
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number880969136DENTIUM007QD 08809460301519 | Date2 Nov 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Laboratory instruments
- Model / Reference
- PDAB4515
- Primary DI / UDI-DI
- 08809460301519
- Basic UDI-DI
- 880969136DENTIUM007QD
- EMDN Code
- L159099 Odontostomatology instruments, reusable - other
- Device Class
- Class I
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- KR-MF-000023279
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
Other devices from Dentium Co., Ltd.
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