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WALLSTENT-Uni™

by Boston Scientific Corporation 26 variants

Ref M001731620

WALLSTENT-Uni™ (M001731620) is a Class III device made by Boston Scientific, registered in EUDAMED on 21 Oct 2026 (Basic UDI-DI B-08714729407133), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-08714729407133 Basic UDI-DI 08714729407133UDI-DIDate21 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
WALLSTENT Uni Endoprosthesis
Model / reference
M001731620
Primary DI / UDI-DI
08714729407133
Basic UDI-DI
B-08714729407133
EMDN code
P070402020101 Stainless steel peripheral vascular bare metal stents
Device class
Class III
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000004702
Authorised representative
Boston Scientific Limited IE-AR-000003840

Other devices from Boston Scientific

See all devices from Boston Scientific →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)