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Sendal, S.L.

Spain ES-MF-000016981 Last updated 17 Sep 2026

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Devices
5
Registries
EUDAMED
FDA recalls
0

Catalogue5

EUDAMED certificates1

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

EUDAMED certificates (1)

TÜV SÜD Product Service GmbH 0123 1 certificate

  • G15 064670 0029 Amended

    Quality management system EU MDR

    Issued
    20 Jul 2026
    Expires
    23 Oct 2027
    Reason
    Other

Notified bodies

About

At BD, we want to usher in a new era of healthcare by bringing medical products, capabilities and solutions to every corner of the world.

Translated from the manufacturer's own website. Source

What Sendal, S.L. makes

Sendal, S.L. manufactures BD Blood Transfusion Sets, designed for the safe administration of blood products in clinical settings.

These devices are classified as Class IIa and are listed in the EU’s eudamed registry. 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 Sendal, S.L. manufacture?

Sendal, S.L. manufactures BD Blood Transfusion Sets, which are specifically designed for the safe administration of blood products in clinical environments. These devices are tailored to support medical procedures where blood transfusions are required.

Where is Sendal, S.L. based?

Sendal, S.L. is based in Spain. The company’s location in Spain aligns it with EU regulatory frameworks, including those governing medical devices.

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

Sendal, S.L.’s BD Blood Transfusion Sets are listed in the EU’s eudamed registry. This database is the official EU portal for medical device information, ensuring transparency and traceability of devices under EU regulations.

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

Sendal, S.L.’s BD Blood Transfusion Sets fall under Class IIa classification in the EU. This classification is assigned based on the risk associated with the device, with Class IIa indicating a moderate risk level that requires conformity assessment procedures to ensure safety and performance.

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

Information

Country
Spain
Address
s/n., Ctra. Nacional Madrid-Caceres, Almaraz, Spain
Website
www.bd.com
Phone
+34927544371
PRRC contact
Juan Antonio Ordiales
EUDAMED SRN
ES-MF-000016981