VUP Medical, a.s.
Czechia CZ-MF-000042015 Last updated 17 Sep 2026
- Devices
- 120
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Knitted vascular prosthesis with collagen Ra lv K Ref 022-20/100
Knitted vascular prosthesis with collagen Ra lv K Ref 022-08/400
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0262
Knitted vascular prosthesis with collagen Ra lv K Ref 022-09/200
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0161
Polypropylene surgical mesh PP MESH (standard 50 g/m2) Ref 091-1205LR
Polypropylene surgical mesh PP MESH (standard 50 g/m2) Ref 091-1406LR
Knitted vascular prosthesis with collagen Ra lv K Ref 022-26/100
Knitted vascular patch with collagen Ra ZK Ref 020-1075
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0181
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0083
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0183
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0164
Knitted vascular prosthesis with collagen Ra lv K Ref 022-10/200
Knitted vascular patch with collagen Ra ZK Ref 020-1010
Knitted vascular prosthesis with collagen Ra lv K Ref 022-30/400
Knitted vascular prosthesis with collagen Ra lv K Ref 022-14/200
Knitted vascular prosthesis with collagen Ra lv K Ref 022-22/300
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0242
Knitted vascular prosthesis with collagen Ra lv K Ref 022-16/300
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0122
Knitted vascular prosthesis with collagen Ra lv K Ref 022-0121
Showing 1-50 of 120
EUDAMED certificates
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
Related companies
Notified bodies
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.
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.
Information
- Country
- Czechia
- Address
- 302/3, Šujanovo náměstí, Brno, Czechia
- Website
- vup.cz/
- [email protected]
- Phone
- +420 543 160 444
- PRRC contact
- Ivana Bátlová
- EUDAMED SRN
- CZ-MF-000042015