VUP Medical, a.s.

CZ-MF-000042015 · Czechia · Brno

VUP Medical, a.s. is registered in the European database on medical devices as a manufacturer, with 201 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Most frequent device types declared: 1. Knitted vascular prosthesis with collagen Ra lv K. 2. Knitted vascu, CORTEX 1 20x50mm, CORTEX 1 40x60mm, CORTEX 2 120x120mm, CORTEX 2 20x25mm.

Among these devices, 201 are declared sterile, 201 implantable.

Devices declared under this manufacturer

• Implantable reinforcing felt for surgical applications CORTEX 1
• Implantable reinforcing felt for surgical applications CORTEX 2
• Implantable reinforcing felt for surgical applications CORTEX 20
• Knitted vascular patch with collagen Ra ZK
• Knitted vascular prosthesis with collagen Ra K
• Knitted vascular prosthesis with collagen Ra K incompressible
• Knitted vascular prosthesis with collagen Ra bv K
• Knitted vascular prosthesis with collagen Ra lv K
• Pletená cévní protéza s kolagenem Ra K
• Polypropylene surgical mesh PP MESH (standard 50g/m2)

Showing 12 of 201 declared devices.

Catalogue references include 022-0223, 022-0261, 022-14/300, 022-30/200, 022-32/400, 024-0714/450.

European nomenclature codes declared: P070102010101, P070102010201, H900302, P07020201, P900202, P070102010101,P070102010201.

United States market access

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Canadian market access

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. VUP Medical, a.s. was not found in either the U.S. or the Canadian register.

Notified body certificates

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