Aesthesio
by Danmic Global, LLC 9 variants
Part of a family of 9 devices: see the family page
Ref 514017
Aesthesio (514017) is a Class I device made by Danmic Global, LLC, registered in EUDAMED on 20 Jan 2026 (Basic UDI-DI 0850006095Aesthesio5R), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number0850006095Aesthesio5R 00850006095353 | Date20 Jan 2026 | StatusActive |
Official records
- EUDAMED public site 0850006095Aesthesio5R
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- Withdrawn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
- Model / reference
- 514017
- Primary DI / UDI-DI
- 00850006095353
- Basic UDI-DI
- 0850006095Aesthesio5R
- Direct marketing DI
- 00850006095353
- EMDN code
- V9099 Various devices not included in other classes - other
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Sweden
Manufacturer details
- EUDAMED SRN
- US-MF-000021060
- Authorised representative
- Code of Practice AB SE-AR-000003002
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