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

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Medicontur Medical Engineering Ltd.

Certificate 2024-MDR/TD-070

Rev. 00Issued
Valid until
Nov 10, 2028

Certificate 2024-MDR/TD-070 is a valid Technical documentation issued to Medicontur Medical Engineering Ltd. and registered in EUDAMED. Valid until November 10, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
2024-MDR/TD-070
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652024-MDR/TD-07000

Validity

Issued
Dec 12, 2024
Valid from
Dec 12, 2024
Valid until
Nov 10, 2028

Notified body

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

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified7

7 scopes

  • Device
    599302A46RFZ
  • Device
    599302A45RT5T
  • Device
    599302A45RD2U9
  • Device
    599302A45DT4H
  • Device
    599302A45SMLWT
  • Device
    599302A4EDF1VG
  • Device
    599302A4EDF2VJ

Documents

LanguagesEN

Manufacturer

Manufacturer
Medicontur Medical Engineering Ltd.
Manufacturer SRN
HU-MF-000024195
Manufacturer country
Hungary

Covered devices

  • 599302A46RFZClass IIb
    599302A46RFZ
  • 599302A45RT5TClass IIb
    599302A45RT5T
  • 599302A45RD2U9Class IIb
    599302A45RD2U9
  • 599302A45DT4HClass IIb
    599302A45DT4H
  • 599302A45SMLWTClass IIb
    599302A45SMLWT
  • 599302A4EDF1VGClass IIb
    599302A4EDF1VG
  • 599302A4EDF2VJClass IIb
    599302A4EDF2VJ

Linked SSCPs

  • SSCP SSCP_01_E