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Resistant

by eucatech AG 42 variants

Ref RSO 07/080-135

Resistant (RSO 07/080-135) is a Class IIb device made by eucatech AG, registered in EUDAMED on 24 May 2024 (Basic UDI-DI B-04251895616883), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04251895616883 Basic UDI-DI 04251895616883UDI-DIDate24 May 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Resistant Peripheral Self-Expandable Stent System
Model / reference
RSO 07/080-135
Primary DI / UDI-DI
04251895616883
Basic UDI-DI
B-04251895616883
EMDN code
P070402020102 Non-stainless steel peripheral vascular bare metal stents
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005541

Similar devices in this category

Other devices filed under NON-STAINLESS STEEL PERIPHERAL VASCULAR BARE METAL STENTS.

Other devices from eucatech AG

See all devices from eucatech AG →

Properties

  • Supplied sterile
  • Implantable
Other properties (10, all answered No)