← Back to catalogue

Z-5

EUDAMED

Class III (EU MDR)

Ref SPT002Model 210Ref SPT003

by NuMED Canada, Inc.

Identity

Trade Name
Z-5 EUDAMED
Z-5 Atrioseptostomy EUDAMED
Device Name
Z-5 Atrioseptostomy EUDAMED
Z-5 Atrioseptostomy Catheter EUDAMED
Model / Reference
210 EUDAMED
SPT002 EUDAMED
SPT003 EUDAMED

Identifiers

Primary DI / UDI-DI
10884117002730 EUDAMED
10884117002723 EUDAMED
Basic UDI-DI
B-10884117002730 EUDAMED
B-10884117002723 EUDAMED
EMDN Code
C0199 ARTERIO-VENOUS DEVICES - OTHER 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-5 by NuMED Canada, Inc. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/MDD

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

Manufacturer

Manufacturer
NuMED Canada, Inc.
EUDAMED SRN
CA-MF-000010949
Authorised Representative
G. van Wageningen B.V. NL-AR-000010437

Sources (2)

  • EUDAMED aace337a-dfad-4340-8ddc-f647c1bb90b3 61 fields · synced Jul 28, 2026
  • EUDAMED 2ebf0411-43d6-46e3-8081-86dc43b22e9b 61 fields · synced May 17, 2026