← Back to catalogue

myoncare

EUDAMED

Class IIa (EU MDR)

Ref ON01039913

by ONCARE GmbH

Identity

Trade Name
myoncare EUDAMED
Device Name
Mobile EUDAMED
Model / Reference
ON01039913 EUDAMED

Identifiers

Primary DI / UDI-DI
04260658860210 EUDAMED
Basic UDI-DI
426065886947238412232007H EUDAMED
Direct Marketing DI
04260658860210 EUDAMED
EMDN Code
Z12040182 GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Germany 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

myoncare by ONCARE GmbH — 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
ONCARE GmbH
EUDAMED SRN
DE-MF-000007460

Sources (1)

  • EUDAMED d3364b93-bbc8-4e66-a2cb-ecba22edb245 61 fields · synced May 22, 2026