FIBRA MOXY - COFEPRIS Registration 882E2021 SSA
Access comprehensive regulatory information for FIBRA MOXY (MOXY FIBER) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 882E2021 SSA and manufactured by BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.. The device was registered on May 25, 2021.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
LA FIBRA DE LÁSER MOXY PRESENTA UNMECANISMO DE EMISIÓN LATERAL QUESUMINISTRAHASTA180WDELUZDE532NMALTEJIDO.LAFIBRAESTÁINDICADAPARALAINCISIÓN/ ESCISIÓN QUIRÚRGICA,VAPORIZACIÓN, ABLACIÓN, HEMOSTASIA YCOAGULACIÓN DE TEJIDO BLANDO. SEINCLUYEN TODOS LOS TEJIDOS BLANDOS,COMO LA PIEL, EL TEJIDO CUTÁNEO, ELTEJIDO SUBCUTÁNEO, LOS TEJIDOS LISOS YESTRIADOS, LOS MÚSCULOS, LOSCARTÍLAGOS, LOS MENISCOS, LASMEMBRANAS MUCOSAS, LOS GANGLIOS YVASOS LINFÁTICOS, LOS ÓRGANOS Y LASGLÁNDULAS
THE MOXY LASER FIBRE FEATURES A LATERAL EMISSION MECHANISM THAT IS SUPPLIED BY 180WOF532NMALWOVEN LIGHT. FIBER IS INDICATED FOR SURGICAL INCISION/EXCISION, VAPORIZATION, ABLATION, HEMOSTASIS, AND SOFT TISSUE COAGULATION. THESE INCLUDE ALL SOFT TISSUES, SUCH AS SKIN, SKIN TISSUE, SUBCUTANEOUS TISSUE, SMOOTH YESTRIATED TISSUES, MUSCLES, CARTILAGE, MENISCI, MUCOUS MEMBRANES, LYMPH NODES AND VESSELS, ORGANS AND GLANDS