Preciso
by Francehopital SAS 4 variants
Ref PREGDMXXXXModel PrecisoPlus
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 | Number805577667PrecisoPlusAU | Date30 May 2025 | StatusActive |
Certificates
No notified-body 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- Withdrawn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
- PrecisoPlus
- Model / Reference
- PrecisoPlus, PREGDMXXXX
- Primary DI / UDI-DI
- 08055776670225
- Basic UDI-DI
- 805577667PrecisoPlusAU
- Direct Marketing DI
- 08055776670225
- EMDN Code
- V0899 Medical support equipment - other
- Device Class
- Class I
- Market of Registration
- Italy
Manufacturer details
- EUDAMED SRN
- FR-MF-000038034
Other devices from Francehopital SAS
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