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ANACONDA BIOMED, S.L.

Spain ES-MF-000009187 Last updated 17 Sep 2026

Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

EUDAMED certificates2

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (2)

Notified body 0344 2 certificates

  • 2266433CE01 Issued

    Quality management system EU MDR

    Issued
    4 Jun 2025
    Expires
    1 Jun 2030
  • 2266433TD01 Issued

    Technical documentation EU MDR

    Issued
    4 Jun 2025
    Expires
    1 Jun 2030

Notified bodies

  • Notified body 0344

About

Anaconda Biomed S.L. is a Barcelona-based medical device start-up developing next-generation endovascular access and protection.

From the manufacturer's own website. Source

What ANACONDA BIOMED, S.L. makes

Anaconda Biomed, S.L. manufactures neurovascular access devices, including the ANA5 Advanced Neurovascular Access and the ANA Advanced Neurovascular Access, designed for endovascular procedures.

These devices are classified as Class III under EU regulations and are listed in the eudamed database. The company is based in Spain.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Anaconda Biomed, S.L. manufacture?

Anaconda Biomed, S.L. specializes in neurovascular access devices. Specifically, they develop products like the ANA5 Advanced Neurovascular Access and the ANA Advanced Neurovascular Access, which are designed to assist in endovascular procedures—interventions performed inside blood vessels, often for treating neurological conditions.

Where is Anaconda Biomed, S.L. based?

The company is headquartered in Barcelona, Spain. This location reflects its focus on developing innovative medical technologies tailored to global endovascular healthcare needs.

Which regulatory registries list Anaconda Biomed, S.L.’s devices?

Anaconda Biomed, S.L.’s devices are listed in the eudamed database, which is the official European Union registry for medical devices. This inclusion ensures transparency and compliance with EU regulatory requirements.

How are Anaconda Biomed, S.L.’s devices classified under EU regulations?

The company’s neurovascular access devices, including the ANA5 and ANA models, fall under Class III classification in the EU. This classification applies to high-risk devices that require stringent regulatory oversight due to their critical role in patient safety and clinical outcomes.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Spain(from SRN)
Address
56, Carrer d'Eivissa, Sant Quirze del Valles, Spain
Website
anaconda.bio/
Phone
+34 933 90 05 08
PRRC contact
Monica Barrett
EUDAMED SRN
ES-MF-000009187