← Back to catalogue

Veriton Ct 316

EUDAMED

Class IIb (EU MDR)

Ref 8010419-01Model VERITON CT

by Spectrum Dynamics Medical SA

Identity

Trade Name
VERITON CT 316 EUDAMED
Device Name
VERITON CT EUDAMED
Model / Reference
VERITON CT EUDAMED
8010419-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07649991184059 EUDAMED
Basic UDI-DI
7649991184VERITON-CTRN EUDAMED
Direct Marketing DI
07649991184059 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 Ct 316 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 84b962c0-dfb4-44d8-9357-b43abb9b1379 61 fields · synced Oct 7, 2026