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Six650hd-E-Gp

EUDAMED

Class IIa (EU MDR)

Ref 62830738

by CMT Medical Technologies, Ltd.

Identity

Trade Name
SIX650HD-E-GP EUDAMED
Device Name
X-Ray Detectors EUDAMED
Model / Reference
62830738 EUDAMED

Identifiers

Primary DI / UDI-DI
07290012104862 EUDAMED
Basic UDI-DI
72900121040372 EUDAMED
Direct Marketing DI
07290012104862 EUDAMED
EMDN Code
Z11031101 MULTIFUNCTIONAL SYSTEMS FOR DIRECT DIGITAL RADIOLOGY EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Category: Stationary basic diagnostic x-ray system, digital

Six650hd-E-Gp by CMT Medical Technologies, Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, digital.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IL-MF-000017569
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 05d51c0a-1729-40c2-9027-30a011f018e5 61 fields · synced Jun 17, 2026