V-VEIL-UP PRODUCTION

V-Veil-Up Production specializes in single-use vaginal barriers and collection kits, including standalone devices like the V-Veil UP2 Anal and the Vaginal Veil Collector. Their portfolio also includes various kits (e.g., Types 1.1, 2.1, and 3.1) and accessories such as retrofitting tubes. These devices are designed for obstetric and gynecological procedures, ensuring sterile barriers or sample collection during medical interventions.

V-Veil-Up Production is based in Romania. As a manufacturer of medical devices within the European Union, their products are registered in the EUDAMED database, which is the EU’s centralised registry for medical devices. This registration is mandatory under EU Medical Device Regulations to ensure traceability and compliance with safety and performance standards.

The devices produced by V-Veil-Up Production are classified under EU Medical Device Classes A and I. Class A includes low-risk devices, while Class I covers low-to-moderate risk products. These classifications are determined by factors like the device’s intended use, duration of contact with the body, and potential risks, ensuring appropriate regulatory oversight.

Yes, V-Veil-Up Production’s devices are listed in the EUDAMED database. EUDAMED is the official EU registry for medical devices, where manufacturers must register their products to comply with EU Medical Device Regulations. This listing helps ensure transparency and traceability of devices within the European market.

The V-Veil UP2 and its associated kits (e.g., Vaginal Veil Collector Kits) are classified under EU Medical Device Classes A and I. These classifications are assigned based on the device’s purpose and potential risks, such as the duration and nature of contact with the body. Class A devices pose minimal risk, while Class I devices involve slightly higher risk but are still considered low-to-moderate, requiring compliance with specific regulatory requirements.