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Ardo Alyssa

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref 63.00.501510(k) K212773

by Ardo medical AG

Identity

Trade Name
Ardo Alyssa EUDAMED
Device Name
Ardo Alyssa EUDAMED
Model / Reference
63.00.501 EUDAMED

Identifiers

Primary DI / UDI-DI
07640108050816 EUDAMED
Basic UDI-DI
B-07640108050816 EUDAMED
EMDN Code
Z12080303 BREAST PUMPS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ardo Alyssa by Ardo medical AG — Class IIa — FDA_510K, MDD — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ardo medical AG
EUDAMED SRN
CH-MF-000016526
Authorised Representative
ARDO medical GmbH DE-AR-000014440

Sources (2)

  • EUDAMED 255d9083-de8b-473f-9db4-1715db7f7022 85 fields · synced Jun 18, 2026
  • FDA 510(k) K212773 1 fields · synced May 18, 2026