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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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Contipro a.s.

Certificate 2025-MDR/QS-033

Rev. 00Issued
Valid until
Aug 4, 2028

Certificate 2025-MDR/QS-033 is a valid Quality management system issued to Contipro a.s. and registered in EUDAMED. Valid until August 4, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
2025-MDR/QS-033
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-03300

Validity

Issued
Jul 10, 2025
Valid from
Jul 10, 2025
Valid until
Aug 4, 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
No
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

No status changes or preceding certificates are recorded.

Scope coverage

Class III2

2 scopes

  • Implantable prosthetic devices - other: Viscoelastic sodium hyaluronate solution (1%) for injection into deep fascia
    Class III
  • DEVICE
    Class III

Manufacturer

Manufacturer
Contipro a.s.
Manufacturer SRN
CZ-MF-000014702
Manufacturer country
Czechia

Covered devices

  • Fascigel HAClass III
    859516379900NY

Documents

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