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Supera™ Peripheral Stent System

by Abbott Medical 110 variants

Ref 42060080-080

Supera™ Peripheral Stent System (42060080-080) is a Class IIb device made by Abbott Medical, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI 8717648PSS00017H), 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 Number8717648PSS00017H Basic UDI-DI 08717648234347UDI-DIDate16 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Peripheral Self-expanding Stent System, Supera
Model / reference
42060080-080
Primary DI / UDI-DI
08717648234347
Basic UDI-DI
8717648PSS00017H
EMDN code
P0704020299 Peripheral vascular stents - other
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000003851
Authorised representative
Abbott Vascular International BE-AR-000002043

Similar devices in this category

Other devices filed under PERIPHERAL VASCULAR STENTS.

Other devices from Abbott Medical

See all devices from Abbott Medical →

Properties

  • Supplied sterile
  • Implantable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
Other properties (12, all answered No)