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Veriton Nm

EUDAMED

Class IIa (EU MDR)

Ref 8010184-01Model 001

by Spectrum Dynamics Medical SA

Identity

Trade Name
VERITON NM EUDAMED
Device Name
VERITON NM SPECT EUDAMED
Model / Reference
001 EUDAMED
8010184-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07649991184011 EUDAMED
Basic UDI-DI
7649991184VERITONLU EUDAMED
Direct Marketing DI
07649991184011 EUDAMED
EMDN Code
Z11020105 FIXED STATION GAMMA CAMERAS WITH MULTIPLE HEADS - WITH ‘TOTAL BODY’ ACQUISITION EUDAMED

Classification

Device Class
Class IIa 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

Veriton Nm by Spectrum Dynamics Medical SA — Class IIa — 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

EUDAMED SRN
CH-MF-000032669
Authorised Representative
SPECTRUM DYNAMICS MEDICAL FRANCE SAS FR-AR-000013226

Sources (1)

  • EUDAMED 0d943f4f-7d3e-4a95-8620-72de234153ed 61 fields · synced Jun 19, 2026