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VitaMD Sperm Analysis System

EUDAMED

Class I (EU MDR)

Ref VitaMD Sperm Analysis System

by VitruvianMD Pte Ltd

Identity

Device Name
VitaMD Sperm Analysis System EUDAMED
Model / Reference
VitaMD Sperm Analysis System EUDAMED

Identifiers

Primary DI / UDI-DI
06009900770611 EUDAMED
Basic UDI-DI
60099007706VitaMDSASC9 EUDAMED
Direct Marketing DI
06009900770611 EUDAMED
EMDN Code
V92 MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Spain 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

VitaMD Sperm Analysis System by VitruvianMD Pte Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
VitruvianMD Pte Ltd
EUDAMED SRN
SG-MF-000049729
Authorised Representative
SigmaTech Nordic ApS DK-AR-000039264

Sources (1)

  • EUDAMED a86626b2-ceb6-4ac2-bd36-d14a83584202 61 fields · synced Jul 12, 2026