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Ardo Alyssa Conversion Kit

EUDAMED

Class IIa (EU MDR)

Ref 63.00.554

by Ardo medical AG

Identity

Trade Name
Ardo Alyssa Conversion Kit EUDAMED
Device Name
Ardo Alyssa EUDAMED
Model / Reference
63.00.554 EUDAMED

Identifiers

Primary DI / UDI-DI
07640108053893 EUDAMED
Basic UDI-DI
B-07640108053893 EUDAMED
EMDN Code
Z12080303 BREAST PUMPS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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 Conversion Kit by Ardo medical AG — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

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 (1)

  • EUDAMED c8344a4d-8b8d-4a45-a2c4-7253c499dda6 61 fields · synced Jul 11, 2026