← Back to catalogue

Z-MEd

EUDAMED

Class III (EU MDR)

Ref PDZ368Model 302.1

by NuMED, Inc.

Identity

Trade Name
Z-MEd EUDAMED
Device Name
Z-MED EUDAMED
Model / Reference
302.1 EUDAMED
PDZ368 EUDAMED

Identifiers

Primary DI / UDI-DI
10887714014953 EUDAMED
Basic UDI-DI
B-10887714014953 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 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
NuMED, Inc.
EUDAMED SRN
US-MF-000010948
Authorised Representative
G. van Wageningen B.V. NL-AR-000010437

Sources (1)

  • EUDAMED d4ba6fd4-3998-4fd5-9dbe-48ef4964e9b4 61 fields · synced May 23, 2026