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Tyshak

EUDAMED

Class III (EU MDR)

Ref SO015Model 102

by NuMED, Inc.

Identity

Trade Name
Tyshak EUDAMED
Device Name
Tyshak EUDAMED
Model / Reference
102 EUDAMED
SO015 EUDAMED

Identifiers

Primary DI / UDI-DI
10887714010467 EUDAMED
Basic UDI-DI
B-10887714010467 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

Tyshak 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 de4d1a97-ba05-49a8-a96f-9cdffb3a8b8e 61 fields · synced May 23, 2026