BodyNeutrAll 5 L
by Vebasan OÜ
Ref EST 00300
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 | Number4280001912BodyNeutrAll2FU 04280001912052 | Date5 Oct 2024 | 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- Withdrawn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
- SkinNeutrAll
- Model / Reference
- EST 00300
- Primary DI / UDI-DI
- 04280001912052
- Basic UDI-DI
- 4280001912BodyNeutrAll2FU
- Direct Marketing DI
- 04280001912052
- EMDN Code
- V9099 Various devices not included in other classes - other
- Device Class
- Class I
- EU market of registration
- Estonia
Manufacturer details
- EUDAMED SRN
- EE-MF-000043782
Other devices from Vebasan OÜ
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