SUTURA PERMATAPE™ - COFEPRIS Registration 1754C2019 SSA
Access comprehensive regulatory information for SUTURA PERMATAPE™ (PERMATAPE™ SUTURE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1754C2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on August 27, 2019.
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.
LA SUTURA PERMATAPE™ ESTÁ INDICADA PARA SU UTILIZACIÓN EN LA APROXIMACIÓN Y/O LIGADURA DE TEJIDOS BLANDOS EN GENERAL, INCLUIDO EL USO CON TEJIDO DE ALOINJERTO PARA PROCEDIMIENTOS ORTOPÉDICOS
THE PERMATAPE™ SUTURE IS INDICATED FOR USE IN THE APPROXIMATION AND/OR LIGATION OF SOFT TISSUES IN GENERAL, INCLUDING USE WITH ALLOGRAFT TISSUE FOR ORTHOPEDIC PROCEDURES