TESI T4MED S.R.L.

TESI T4MED S.R.L. manufactures reusable surgical instruments and systems, including the Entry+, a reusable surgical instrument, the Octopus, a surgical retractor system, the eViSuS BioCare, a reusable surgical instrument with bio-cleaning capabilities, and the Master, designed for specific surgical procedures. These devices are intended for use in operating rooms to assist surgeons during procedures.

TESI T4MED S.R.L. is based in Italy. The company’s location in Italy aligns with its focus on manufacturing medical devices that comply with European Union regulations.

Yes, TESI T4MED S.R.L.’s devices are listed in the eudamed registry, which is the European Union’s centralised database for medical devices. Listing in eudamed ensures transparency and traceability of devices authorised under EU regulations.

TESI T4MED S.R.L.’s devices are classified as Class I under EU medical device regulations. This classification applies to devices posing minimal risk, such as reusable surgical instruments and retractors, which typically require less stringent regulatory scrutiny than higher-risk devices.