Skip to content

Supolene

by Advanced Medical Solutions (France) SAS 218 variants

Ref W520

Supolene (W520) is a Class IIb device made by Advanced Medical Solutions (France) SAS, registered in EUDAMED on 21 Aug 2026 (Basic UDI-DI 3661522TDSU3401XN), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3661522TDSU3401XN Basic UDI-DI 03661522120156UDI-DIDate21 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Supolene
Model / reference
W520
Primary DI / UDI-DI
03661522120156
Basic UDI-DI
3661522TDSU3401XN
EMDN code
H010201020203 Polyester multifilament without needle
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000000666

Similar devices in this category

Other devices filed under POLYESTER MULTIFILAMENT WITHOUT NEEDLE.

Other devices from Advanced Medical Solutions (France) SAS

See all devices from Advanced Medical Solutions (France) SAS →

Properties

  • Supplied sterile
  • Sterilise before use
  • Implantable
  • Sutures
Other properties (11, all answered No)