EU → North America 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: ADA Swabs, Gauze roll, Incontinence diapers, Incontinence underpads, Non-sterile crepe bandages.

Among these devices, 1 177 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 1 885 declared devices.

Catalogue references include 00010180200000, 00170005050898, 00170245450401-1, 00170510200809, 00170550500400, 00500510100400.

European nomenclature codes declared: M0201020101, M0201020201, M0202010101, M0201020102, M0201020202, M0202010102.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED1 885
Country of registrationPortugal

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN1 885
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. Albino Dias de Andrade, S.A. was not found in either the U.S. or the Canadian register.

Notified body certificates

CertificateStatusExpiry
ES25/00000301supplemented2030-03-13

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