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VUP Medical, a.s.

Czechia CZ-MF-000042015 Last updated 17 Sep 2026

Devices
120
Registries
EUDAMED
FDA recalls
0

Catalogue120

Page 1 of 3

Showing 1-50 of 120

EUDAMED certificates6

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (6)

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

  • 1434-MDR-001/2025 Issued

    Quality management system EU MDR

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

    Technical documentation EU MDR

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

    Quality management system EU MDR

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

    Technical documentation EU MDR

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

    Quality management system EU MDR

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

    Technical documentation EU MDR

    Issued
    4 Mar 2025
    Expires
    3 Mar 2030

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.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does VUP Medical, a.s. manufacture?

VUP Medical, a.s. specializes in producing knitted vascular prostheses reinforced with collagen. These devices are designed specifically for vascular reconstruction surgeries, replacing or reinforcing blood vessels. The prostheses come in various forms, including both incompressible and compressible variants, as well as low-volume (lv) and high-volume (bv) configurations, to suit different surgical needs.

Where is VUP Medical, a.s. based, and where are its devices registered?

VUP Medical, a.s. is based in the Czech Republic (CZ). Its devices are registered in the EUDAMED database, which is the European Union’s medical device registry. This registration ensures compliance with EU regulatory requirements for medical devices, including traceability and transparency for authorized products.

How are the vascular prostheses manufactured by VUP Medical classified under EU regulations?

The vascular prostheses produced by VUP Medical are classified as either Class IIb or Class III medical devices under EU regulations. This classification is determined by factors such as the device’s risk level, intended use, and potential impact on patient safety. Class III devices are typically high-risk implants, such as vascular prostheses, which require rigorous evaluation to ensure safety and performance.

Are VUP Medical’s devices listed in any other regulatory registries besides EUDAMED?

Based on the available information, VUP Medical’s devices are registered in the EUDAMED database. EUDAMED is the primary EU-wide registry for medical devices, ensuring transparency and compliance with EU regulations. No other registries are mentioned in the provided data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Czechia
Address
302/3, Šujanovo náměstí, Brno, Czechia
Website
vup.cz/
Phone
+420 543 160 444
PRRC contact
Ivana Bátlová
EUDAMED SRN
CZ-MF-000042015