HABIB ENDOHPB - COFEPRIS Registration 570C2020 SSA
Access comprehensive regulatory information for HABIB ENDOHPB (HABIB ENDOHPB) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 570C2020 SSA and manufactured by BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.. The device was registered on May 28, 2020.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
EL DISPOSITIVO HABIB ENDOHPB ESTÁINDICADO PARA SU USO EN LA ABLACIÓNPARCIALOTOTALDELTEJIDOENELCONDUCTOPANCREÁTICO Y BILIAR, TAMBIÉN ESTÁPREVISTOPARAEXTIRPARTEJIDOMALIGNOOBENIGNO, PARA REALIZAR DRENAJE ODESCOMPRESIÓNBILIARENDOSCÓPICA,ANTESDE LA COLOCACIÓN DEL STENT O DESPUÉS,PARA DESPEJAR EL STENT OCLUIDO.
THE HABIB ENDOHPB DEVICE IS INDICATED FOR USE IN PARTIAL OR TOTAL ABLATION OF TISSUE IN THE PANCREATIC AND BILIARY DUCT, IT IS ALSO INTENDED TO REMOVE MALIGNANT OR BENIGN ARTEJIDO, TO PERFORM ENDOSCOPIC BILIARY DRAINAGE OR DECOMPRESSION, BEFORE STENT PLACEMENT OR AFTER, TO CLEAR THE OCCLUDED STENT.