← Back to catalogue

Hativ P30

EUDAMED

Class IIa (EU MDR)

Ref Hativ P30BModel Hativ P30A, Hativ P30B

by VUNO Inc.

Identity

Device Name
HATIV P30 EUDAMED
Model / Reference
Hativ P30A, Hativ P30B EUDAMED
Hativ P30B EUDAMED

Identifiers

Primary DI / UDI-DI
08800045800236 EUDAMED
Basic UDI-DI
88000458HTPY5 EUDAMED
Direct Marketing DI
08800045800236 EUDAMED
EMDN Code
Z12050301 GENERAL PURPOSE ELECTROCARDIOGRAPHS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Hativ P30 by VUNO Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

Manufacturer
VUNO Inc.
EUDAMED SRN
KR-MF-000022266
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 8b9042ae-f217-41fa-8f93-c67d612d4a14 61 fields · synced Jun 18, 2026