MD Atlas
BlogPricingSign in
MD Atlas
Made In Tracker
Made In TrackerEasyUDI
Legal
Privacy PolicyLegal Notice
About
AboutFAQGlossaryBlogMCP serverPartnersContact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

  • MD Atlas
  • Documents

DEYMED Diagnostic s.r.o.

Certificate 2024-MDR/QS-066

Rev. 01Supplemented
Valid until
Dec 12, 2029

Certificate 2024-MDR/QS-066 is a valid Quality management system issued to DEYMED Diagnostic s.r.o. and registered in EUDAMED. Valid until December 12, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
2024-MDR/QS-066
Certificate type
Quality management system
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
2
Certificate ID
22652024-MDR/QS-06601

Validity

Issued
Mar 12, 2025
Valid from
Mar 12, 2025
Valid until
Dec 12, 2029

Notified body

Notified body
3EC International a.s.
Notified body SRN
2265
Notified body country
Slovakia

Characteristics

Sterile
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
No
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Basic UDI-DI data only

History

Status changes

  • Supplemented

Supersedes

  • 2024-MDR/QS-066Quality management systemIssuedDec 12, 2024 → Dec 12, 2029

Scope coverage

Class IIa4

4 scopes

  • Magnetic stimulators - DuoMAG XT
    Class IIa
  • Magnetic stimulators - DuoMAG XTR
    Class IIa
  • Magnetic stimulators - DuoMAG MP
    Class IIa
  • DEVICE
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
DEYMED Diagnostic s.r.o.
Manufacturer SRN
CZ-MF-000001824
Manufacturer country
Czechia

Covered devices

  • DuoMAGClass IIa
    8592566-DM-000018L