Examination and Treatment Couch
by Plinth Medical Ltd 83 variants
Ref 502RModel 500 Series
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 | Number506064329STANDARDZ9 05060643290621 | Date11 Aug 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- Withdrawn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
- Device Name
- Examination and Treatment Couch
- Model / Reference
- 500 Series, 502R
- Primary DI / UDI-DI
- 05060643290621
- Basic UDI-DI
- 506064329STANDARDZ9
- EMDN Code
- V080603 Treatment, diagnosis and monitoring medical beds
- Device Class
- Class I
- EU market of registration
- Malta
Manufacturer details
- EUDAMED SRN
- UK-MF-000057774
- Authorised representative
- Advena Limited MT-AR-000000234
Other devices from Plinth Medical Ltd
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