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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 2023-MDR/TD-016

Rev. 0Issued
Valid until
Aug 4, 2028

Overview

Certificate number
2023-MDR/TD-016
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652023-MDR/TD-0160

Validity

Issued
Aug 4, 2023
Valid from
Aug 4, 2023
Valid until
Aug 4, 2028

Manufacturer

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

Notified body

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

Covered devices

  • Sicalm HAClass III
    859516377700N8

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

Unspecified1

1 scope

  • Sicalm HA
    859516377700N8

Documents

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