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Z-Med Ii-X

EUDAMED

Class III (EU MDR)

Ref PDZ724Model 305X

by NuMED, Inc.

Identity

Trade Name
Z-MED II-X EUDAMED
Device Name
Z-MED II-X EUDAMED
Model / Reference
305X EUDAMED
PDZ724 EUDAMED

Identifiers

Primary DI / UDI-DI
10887714019613 EUDAMED
Basic UDI-DI
B-10887714019613 EUDAMED
EMDN Code
C019014 CARDIAC VALVULOPLASTY CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

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

Z-Med Ii-X by NuMED, Inc. — Class III — 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
NuMED, Inc.
EUDAMED SRN
US-MF-000010948
Authorised Representative
G. van Wageningen B.V. NL-AR-000010437

Sources (1)

  • EUDAMED 4e901f44-1fd1-4a6f-af66-0b81cd736dbe 61 fields · synced Jun 20, 2026