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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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MEDIN, a.s.

Certificate 2025-MDR/QS-084

Rev. 00Issued
Valid until
Aug 31, 2028

Certificate 2025-MDR/QS-084 is a valid Quality management system issued to MEDIN, a.s. and registered in EUDAMED. Valid until August 31, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
2025-MDR/QS-084
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652025-MDR/QS-08400

Validity

Issued
Dec 22, 2025
Valid from
Dec 22, 2025
Valid until
Aug 31, 2028

Notified body

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

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb6

6 scopes

  • BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS
    Class IIb
  • CANNULATED SCREWS
    Class IIb
  • DEVICE
    Class IIb
  • DEVICE
    Class IIb
  • DEVICE
    Class IIb
  • DEVICE
    Class IIb

Documents

LanguagesEN

Manufacturer

Manufacturer
MEDIN, a.s.
Manufacturer SRN
CZ-MF-000012371
Manufacturer country
Czechia

Covered devices

  • Headless screwClass IIb
    85917126030501WE
  • Headless screw sterileClass IIb
    85917126030501SQ5
  • Bone screwClass IIb
    85917126030101VS
  • Bone screw sterileClass IIb
    85917126030101SP9

Linked SSCPs

  • SSCP 6.3.5.1_SSCP_EN