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Veriton Ct16

EUDAMED

Class IIb (EU MDR)

Ref 8010172-01Model VERITON CT

by Spectrum Dynamics Medical SA

Identity

Trade Name
VERITON CT16 EUDAMED
VERITON CT 216 EUDAMED
Device Name
VERITON CT EUDAMED
Model / Reference
VERITON CT EUDAMED
8010172-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07649991184035 EUDAMED
Basic UDI-DI
7649991184VERITON-CTRN EUDAMED
Direct Marketing DI
07649991184035 EUDAMED
EMDN Code
Z11020201 CT/GAMMA CAMERA SYSTEMS EUDAMED

Classification

Device Class
Class IIb 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 Ct16 by Spectrum Dynamics Medical SA — Class IIb — 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 (2)

  • EUDAMED 822cf34e-70e3-446c-8505-23d966024b41 61 fields · synced Jun 18, 2026
  • EUDAMED 2aa7c0bf-2367-4ab5-932a-808861770a6a 61 fields · synced Jun 18, 2026