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AMDS Hybrid Prosthesis

by Ascyrus Medical GmbH 5 variants

Ref AMDS40Model Ascyrus Medical Dissection Stent Hybrid Prosthesis

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-87723400AMDS4055MRAH Basic UDI-DI D-87723400AMDS4055MRAHUDI-DIDate25 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

LithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicAustriaHungarySloveniaSpainItalyCroatiaGreece
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 16 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 1 Jan 2019
  • Belgium since 1 Jan 2019
  • Croatia since 1 Jan 2019
  • Czechia since 1 Jan 2019
  • France since 1 Jan 2019
  • Germany since 1 Jan 2019
  • Greece since 1 Jan 2019
  • Hungary since 1 Jan 2019
  • Ireland since 1 Jan 2019
  • Italy since 1 Jan 2019
  • Lithuania since 1 Jan 2019
  • Luxembourg since 1 Jan 2019
  • Netherlands since 1 Jan 2019
  • Poland since 1 Jan 2019
  • Slovenia since 1 Jan 2019
  • Spain since 1 Jan 2019

Last checked 29 Oct 2026.

Specification

EUDAMED

Device Name
Ascyrus Medical Dissection Stent Hybrid Prosthesis
Model / Reference
Ascyrus Medical Dissection Stent Hybrid Prosthesis, AMDS40
Primary DI / UDI-DI
D-87723400AMDS4055MRAH
Basic UDI-DI
B-87723400AMDS4055MRAH
EMDN Code
P070402020102 Non-stainless steel peripheral vascular bare metal stents
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000023621

From the manufacturer

Manufacturer's product page: AMDS™

Other devices from Ascyrus Medical GmbH

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (8)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No