Contipro a.s.

Certificate 2025-MDR/TD-033

Rev. 00Issued

Valid until: Aug 4, 2028

Certificate 2025-MDR/TD-033 is a valid Technical documentation 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/TD-033
Certificate type: Technical documentation
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 22652025-MDR/TD-03300

Validity

Issued: Jul 10, 2025
Valid from: Jul 10, 2025
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

Fascigel HAClass III
859516379900NY

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

Fascigel HA
859516379900NY

Documents

LanguagesCSEN