Euphoria Plus
by Orthos XXI, Unipessoal Lda 2 variants
Ref 55CM3EULT, 55CMEUCONFIG, 55CM3EUPLModel Euphoria
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 | Number56004569EUPHORIAEP9 | Date26 Mar 2026 | StatusActive |
Certificates
No certifier 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- Withdrawn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
- Trade Name
- Euphoria PlusEuphoria
- Device Name
- Cama Hospitalar Elétrica
- Model / Reference
- Euphoria, 55CM3EULT, 55CMEUCONFIG, 55CM3EUPL
- Primary DI / UDI-DI
- 05600456970299, 05600456970251, 05600456970305
- Basic UDI-DI
- 56004569EUPHORIAEP9
- Direct Marketing DI
- 056004569702990560045697025105600456970305
- EMDN Code
- V08060102 Intensive care or resuscitation electric medical beds
- Device Class
- Class I
- EU market of registration
- Portugal
Manufacturer details
- EUDAMED SRN
- PT-MF-000002787
Other devices from Orthos XXI, Unipessoal Lda
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