Nctf 135 Ha
Ref 3F4010
Active
CE MDR
Valid until
6 Jan 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberEPT 0477.MDR.25/5692 | Date7 Jan 2025 | StatusActive |
Certificates
- EPT 0477.MDR.25/5692 Active
Technical documentation EU MDR
- Certifier
- Eurofins Product Testing Italy S.r.l. 0477
- Issued
- 7 Jan 2025
- Expires
- 6 Jan 2030
- EPT 0477.MDR.25/5693 Active
Quality management system EU MDR
- Certifier
- Eurofins Product Testing Italy S.r.l. 0477
- Issued
- 7 Jan 2025
- Expires
- 6 Jan 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- 3F4010
- Primary DI / UDI-DI
- 03664948000859
- Basic UDI-DI
- 3664948NCTF135HADN
- EMDN Code
- X0301 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, excluding those for tattooing – resorbable
- Device Class
- Class III
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000007907
Other devices from Laboratoires Fill-Med
Properties
Other properties (11)
- 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