Fig. 22
by Medspo
Ref MD1009Model MD1025
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number++G520MD1025K3 ++G520MD1009K5 | Date15 Aug 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Dental Extracting Forceps
- Model / reference
- MD1025, MD1009
- Primary DI / UDI-DI
- ++G520MD1009K5
- Basic UDI-DI
- ++G520MD1025K3
- EMDN code
- L150301 Dental extraction tooth forceps, reusable
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- PK-MF-000037594
- Authorised representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Other devices from Medspo
Properties
Other properties (12)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No