Filldermal W22
Ref ITF005/cModel Linea SKIN-F
Active
CE MDR
Valid until
2 Mar 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberCSQ0006237126 | Date30 Apr 2026 | StatusActive |
Certificates
- CSQ0006237126 Active
Quality management system EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 30 Apr 2026
- Expires
- 2 Mar 2028
- Reason
- Add device or group
- CVD0042250826 Active
Technical documentation EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 30 Apr 2026
- Expires
- 2 Mar 2028
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Skin-F 22
- Model / Reference
- Linea SKIN-F, ITF005/c
- Primary DI / UDI-DI
- 08055715335857
- Basic UDI-DI
- 805571533ITF00578abdYB
- Direct Marketing DI
- 08055715335857
- EMDN Code
- P900402 Resorbable filling and reconstruction devices
- Device Class
- Class III
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000013116
Other devices from Italfarmacia srl
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