Benostan Health Products Venocontract Emulsion
Ref 120325md
Active
CE MDR CE MDD
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 | NumberB-5206172203255RN | Date18 Apr 2022 | StatusActive |
| European Union | CE/MDD | NumberB-5206172203255RN | Date18 Apr 2022 | 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- Withdrawn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, CE/MDD Active
Specification
- Trade Name
- Benostan Health Products Venocontract EmulsionBenostan Venocontract Emulsion
- Model / Reference
- 120325md
- Primary DI / UDI-DI
- D-5206172203255RN, 05206172203255
- Basic UDI-DI
- B-5206172203255RN, 52061721GR800349168FA
- Direct Marketing DI
- 05206172203255
- EMDN Code
- M9002 Protective devices, lubricants and soothing devices (sprays, gels, fluids and creams)
- Device Class
- Class I
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- GR-MF-000021200
Other devices from Benostan Health Products Ανωνυμη Εταιρεια Παραγωγης Και Εμποριας Καλλυντικων, Φαρμακευτικων Και Συναφων Προιοντων / Benostan Health Products Α.Ε.
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