NEURIMPULSE S.R.L.

NeuImpulse S.r.l. manufactures devices under the NEURIMPULSE brand, which are likely medical electrical stimulation or neuromodulation systems. These devices are designed for therapeutic or diagnostic purposes in areas such as neurological or musculoskeletal applications, though the exact use cases are not specified in the provided data.

NeuImpulse S.r.l. is based in Italy, as indicated in the company’s registration details. This location is relevant for regulatory compliance, particularly under EU medical device regulations.

NeuImpulse S.r.l.’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical device information. This registry is used for transparency and compliance tracking under EU medical device legislation.

NeuImpulse S.r.l.’s devices fall under EU Class I classification. This classification is typically assigned to low-risk medical devices, such as some diagnostic tools or non-invasive therapeutic devices, though the specific risk assessment would depend on the device’s intended purpose and design.