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VUP Medical, a.s.

Active in EUDAMED

Czechiafrom SRN EUDAMED SRN CZ-MF-000042015

Devices
121
Registrations
EUDAMED

What VUP Medical, a.s. makes

VUP Medical produces knitted vascular prostheses reinforced with collagen, designed for vascular reconstruction. These include both incompressible and compressible variants, tailored for specific surgical applications in blood vessel replacement. The prostheses are available in multiple configurations, including low-volume (lv) and high-volume (bv) variants, to accommodate different anatomical requirements.

The company’s vascular prostheses are classified as Class IIb and Class III medical devices under EU regulations, with all relevant products registered in the EUDAMED database. These devices are intended for use within the European Union and adhere to the applicable regulatory standards for surgical implants.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Company details

EUDAMED SRN
CZ-MF-000042015
EU VAT number
CZ15546578
EUDAMED status
Active
EUDAMED registered name
VUP Medical, a.s.
Registered address
302/3, Šujanovo náměstí, 602 00, Brno, Czechia
Website
vup.cz/
Phone
+420 543 160 444
PRRC contact
Ivana Bátlová(public in EUDAMED)

EUDAMED certificates6

6 certificates6 valid, 0 expiredMDR 6next expiry 3 Mar 2030

EUDAMED certificates (6)

POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. 1434 6 certificates

  • 1434-MDR-001/2025 Active

    Quality management system EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030
  • 1434-MDR-002/2025 Active

    Technical documentation EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030
  • 1434-MDR-003/2025 Active

    Quality management system EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030
  • 1434-MDR-004/2025 Active

    Technical documentation EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030
  • 1434-MDR-007/2025 Active

    Quality management system EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030
  • 1434-MDR-008/2025 Active

    Technical documentation EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030