SLH DC Temporary PEEK Abutment Hex
Ref DC 32022Model DC Superstructures
Active
CE MDR CE MDD
Valid until
15 Jun 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number2975-MED-2616701 | Date16 Jun 2026 | StatusActive |
| European Union | CE/MDD | NumberB-04260662230962 | Date26 Oct 2022 | StatusActive |
Certificates
- 2975-MED-2616701 Active
Quality management system EU MDR
- Notified body
- SZUTEST Konformitätsbewertungsstelle GmbH 2975
- Issued
- 16 Jun 2026
- Expires
- 15 Jun 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Trade Name
- SLH DC Temporary PEEK Abutment HexSLH DC Temporary Abutment (HEX) Ø 5.0 mm
- Device Name
- Temporary PEEK Abutment HexSLH DC Temporary Abutment
- Model / Reference
- DC 32022, DC Superstructures
- Primary DI / UDI-DI
- 04260662230962
- Basic UDI-DI
- B-04260662230962, 426066223TAQQ
- Direct Marketing DI
- 04260662230962
- EMDN Code
- P01020180 Dental implants - accessories
- Device Class
- Class IIb
- Market of Registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000020864
Other devices from SLH Microtech GmbH
Properties
Other properties (12)
- Sterile: 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