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Scitech Produtos Médicos SA

Certificate 2025-MDR/QS-015

Rev. 00Issued
Valid until
Feb 7, 2030

Certificate 2025-MDR/QS-015 is a valid Quality management system issued to Scitech Produtos Médicos SA and registered in EUDAMED. Valid until February 7, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
2025-MDR/QS-015
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-01500

Validity

Issued
Feb 7, 2025
Valid from
Feb 7, 2025
Valid until
Feb 7, 2030

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 IIb2

2 scopes

  • PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - PERIPHERAL
    Class IIb
  • DEVICE
    Class IIb

Documents

LanguagesEN

Manufacturer

Manufacturer
Scitech Produtos Médicos SA
Manufacturer SRN
BR-MF-000018627
Manufacturer country
Brazil

Covered devices

  • Vascular Stent GraftClass IIb
    79082497SOLARISCB