Neuramis Deep Lidocaine
by Medytox Inc.
Active
CE MDR
Valid until
1 Apr 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number880613800003DA 08806138000033 | Date15 Apr 2026 | StatusActive |
Certificates
- MDR.2292-2026/0013 Active
Technical documentation EU MDR
- Certifier
- UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş. 2292
- Issued
- 2 Apr 2026
- Expires
- 1 Apr 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Primary DI / UDI-DI
- 08806138000033
- Basic UDI-DI
- 880613800003DA
- EMDN Code
- X0303 Substances, combinations of substances, or items without an intended medical purpose intended to be used for facial or other dermal or mucous membrane filling by subcutaneous, submucous or intradermal injection or other introduction, by a prefilled means for introduction, excluding those for tattooing – resorbable
- Device Class
- Class III
- EU market of registration
- Sweden
Manufacturer details
- EUDAMED SRN
- KR-MF-000028153
- Authorised representative
- Obelis s.a. BE-AR-000000106
Properties
Other properties (10)
- 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