NEW ANCORVIS SRL

New Ancorvis SRL specializes in dental implant components, including abutments and prosthetic bases. Their portfolio includes titanium-based and cobalt-chromium abutments, such as the MUA (Multi Unit Abutment) series and Mbase F.A.S., as well as base units for implant systems like the V4 System Base and LINK IN Ti Base. These devices are designed for dental prosthetics and multi-unit attachments.

New Ancorvis SRL is based in Italy, which means its devices must comply with the European Union’s Medical Device Regulations (MDR). The company’s products are listed in the EUDAMED database, a transparency tool for medical devices within the EU, ensuring they meet regulatory requirements for distribution and use in the European market.

New Ancorvis SRL’s devices are classified under the EU Medical Device Regulations as Class I, Class IIa, or Class IIb. The classification depends on factors like the device’s risk level, intended use, and potential impact on patient safety. For example, abutments and prosthetic bases for dental implants are typically assigned higher classifications (Class IIa or IIb) due to their direct contact with the body and functional role in restoring dental function.

Yes, New Ancorvis SRL’s devices are listed in the EUDAMED database, which is the European Union’s transparency tool for medical devices. Listing in EUDAMED confirms that the devices have undergone the necessary regulatory processes to comply with EU Medical Device Regulations. This transparency helps healthcare professionals, regulators, and patients verify the device’s legal status and compliance before use.