Alma C Fp +21
by Almax Imaging srl 10 variants
Ref 11.01.800.008, 11.01.800.003, 11.01.800.004, 11.01.800.007, 11.01.800.005, 11.01.800.014, 11.01.800.015Model ALMA C FP +21
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number805618229ALMAC9Y | Date24 Feb 2024 | 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- Withdrawn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
- Alma C Fp +21
- Model / Reference
- ALMA C FP +21, 11.01.800.008, 11.01.800.003, 11.01.800.004, 11.01.800.007, 11.01.800.005, 11.01.800.014, 11.01.800.015
- Primary DI / UDI-DI
- 08056182290137, 08056182290083, 08056182290090, 08056182290120, 08056182290106, 08056182290199, 08056182290205
- Basic UDI-DI
- 805618229ALMAC9Y
- Direct Marketing DI
- 08056182290137080561822900830805618229009008056182290120080561822901060805618229019908056182290205
- EMDN Code
- Z11039017 Mobile radioscopic units
- Device Class
- Class IIb
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000028923
Other devices from Almax Imaging srl
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