Symmcora permanent
by Assut Europe SpA 38 variants
Ref G4010AAB
Symmcora permanent (G4010AAB) is a Class III device made by Assut Europe SpA, registered in EUDAMED on 6 Nov 2024 (Basic UDI-DI 8033439FILBLOCPERMHW) with CE/MDR certificate CSQ0013236826 valid until 7 Aug 2028, active as of 24 Oct 2026.
Active
CE MDR
Valid until
7 Aug 2028
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberCSQ0013236826 | Date26 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 8033439FILBLOCPERMHW
Certificates
- CSQ0013236626 Active
Quality management system EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 28 Sep 2026
- Expires
- 7 Aug 2028
- Reason
- Add device or group
- CSQ0013236826 Active
Quality management system EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 26 Oct 2026
- Expires
- 7 Aug 2028
- Reason
- Add device or group
- CVD0030240124 Active
Technical documentation EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 31 Jul 2024
- Expires
- 7 Aug 2028
- Reason
- Add device or group
Timeline
- Certificate issued EUDAMED CVD0030240124
- Registered EUDAMED 8033439FILBLOCPERMHW
- Certificate issued EUDAMED CSQ0013236826
- Certificate expires EUDAMED CSQ0013236826
- Certificate expires EUDAMED CVD0030240124
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
- Spain
Specification
- Device name
- Filbloc Permanent
- Model / reference
- G4010AAB
- Primary DI / UDI-DI
- 18033439376476
- Basic UDI-DI
- 8033439FILBLOCPERMHW
- Direct marketing DI
- 18033439376476
- EMDN code
- H010201010401 Polypropylene monofilament with needle for open surgery
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- IT-MF-000018178
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