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Myrian® 2.13 : Platform

EUDAMED

Class IIa (EU MDR)

Ref Myrian® 2.13 : PlatformModel Myrian

by Intrasense

Identity

Trade Name
Myrian® 2.13 : Platform EUDAMED
Device Name
Myrian EUDAMED
Model / Reference
Myrian EUDAMED
Myrian® 2.13 : Platform EUDAMED

Identifiers

Primary DI / UDI-DI
03700719700754 EUDAMED
Basic UDI-DI
37007197MyrianGW EUDAMED
Direct Marketing DI
03700719700754 EUDAMED
EMDN Code
Z11069005 DIAGNOSTIC IMAGING WORKSTATIONS EUDAMED

Classification

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Tissue specimen x-ray system IVD

Myrian® 2.13 : Platform by Intrasense — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tissue specimen x-ray system IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Intrasense
EUDAMED SRN
FR-MF-000001551

Sources (1)

  • EUDAMED 11835541-1003-432a-ba26-c4e13d22886b 61 fields · synced Jun 18, 2026