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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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MD Atlas
Documents

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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