UF(II) DeSR Base Abutment
by DIO Corporation 108 variants
Ref DSRBA 6501H
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 | Number880004925005B8 08800049467947 | Date23 Oct 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- Withdrawn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
- UF Implant Prosthetic Components
- Model / reference
- DSRBA 6501H
- Primary DI / UDI-DI
- 08800049467947
- Basic UDI-DI
- 880004925005B8
- EMDN code
- P01020180 Dental implants - accessories
- Device class
- Class IIb
- EU registration type
- Standard device
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- KR-MF-000008515
- Authorised representative
- AR Experts B.V. NL-AR-000023989
Other devices from DIO Corporation
Properties
Other properties (12)
- Supplied sterile: No
- Reusable: 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