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Amaryll Plus

EUDAMED

Class IIa (EU MDR)

Ref 63.00.319

by Ardo medical AG

Identity

Trade Name
AMARYLL PLUS EUDAMED
Device Name
Amaryll EUDAMED
Model / Reference
63.00.319 EUDAMED

Identifiers

Primary DI / UDI-DI
07640109055872 EUDAMED
Basic UDI-DI
B-07640109055872 EUDAMED
EMDN Code
V020301 MANUAL BREAST PUMPERS AND KITS 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

Amaryll Plus 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 de3f3b4e-3bb4-4737-9b5e-73c034b11572 61 fields · synced Jun 18, 2026