EU → US Device Access

Albino Dias de Andrade, S.A.

PT-MF-000002823 · Portugal · Seroa

Albino Dias de Andrade, S.A. is registered in the European database on medical devices as a manufacturer, with 1 885 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa1 885

Most frequent device types declared: Sterile gauze and non-woven dressings without XR contrast thread, Sterile gauze and non-woven dressings with XR contrast thread, Non-sterile gauze and non-woven dressings without XR contrast thread, ADA Swabs, Non-sterile crepe bandages.

Among these devices, 1 177 are declared sterile.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED1 885
Country of registrationPortugal
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

Notified body certificates

CertificateStatusExpiry
ES25/00000301supplemented2030-03-13

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