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Endospan Ltd

Active in EUDAMED

Israelfrom SRN EUDAMED FDA SRN IL-MF-000014169 FEI 3009304068

Devices
132
Registrations
EUDAMEDFDA
FDA recalls
0

What Endospan Ltd makes

Endospan, Ltd. manufactures the NEXUS Aortic Arch Stent Graft System, a device designed for endovascular repair of aortic arch aneurysms and complex aortic pathologies. The system is intended to provide structural support and exclude blood flow from the aneurysm sac while maintaining patency of the true lumen.

The NEXUS Aortic Arch Stent Graft System is classified as a Class III medical device under FDA regulations and is listed under a Premarket Approval (PMA) application. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Company details

EUDAMED SRN
IL-MF-000014169
FDA FEI number
3009304068
DUNS number
532700825
EUDAMED status
Active
EUDAMED registered name
Endospan Ltd
Registered address
4, Maskit St., 4673304, Herzliya, Israel
Phone
+972-9-7884620
PRRC contact
Shiran Mor Yossef(public in EUDAMED)

EUDAMED certificates2

2 certificates2 valid, 0 expiredMDR 2next expiry 11 Feb 2031

EUDAMED certificates (2)

TÜV SÜD Product Service GmbH 0123 2 certificates

  • G70 132171 0004 Active Supplemented

    Technical documentation EU MDR

    Issued
    12 Oct 2026
    Expires
    23 Jun 2031
    Reason
    Add device or group
  • G15 132171 0003 Active Supplemented

    Quality management system EU MDR

    Issued
    30 Jul 2026
    Expires
    11 Feb 2031
    Reason
    Add device or group