Resolon®
by Advanced Medical Solutions (France) SAS 161 variants
Ref 88062
Resolon® (88062) is a Class IIb device made by Advanced Medical Solutions (France) SAS, registered in EUDAMED on 19 Aug 2026 (Basic UDI-DI 3661522TDSU3201XC), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number3661522TDSU3201XC 03661522125274 | Date19 Aug 2026 | StatusActive |
Official records
- EUDAMED public site 3661522TDSU3201XC
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- 88062
- Primary DI / UDI-DI
- 03661522125274
- Basic UDI-DI
- 3661522TDSU3201XC
- EMDN code
- H010201010101 Polyamide monofilament with needle
- Device class
- Class IIb
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- FR-MF-000000666
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