INVOCELL™ - COFEPRIS Registration 119C2021 SSA
Access comprehensive regulatory information for INVOCELL™ (INVOCELL™) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 119C2021 SSA and manufactured by EMERGO,S.DER.L.DEC.V.. The device was registered on February 02, 2021.
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 SISTEMA DE CULTIVO INTRAVAGINALINVOCELL™ CONSISTE EN LOSCOMPONENTES SIGUIENTES: EL USO DELSISTEMADECULTIVOESTÁINDICADOENLAPREPARACIÓN, RETENCIÓN YTRANSFERENCIADEGAMETOSOEMBRIONESHUMANOS DURANTE LOS PROCEDIMIENTOSDE FECUNDACIÓN IN VITRO/ CULTIVOINTRAVAGINAL IN VITRO (INVITROFERTILIZATION/INTRAVAGINAL CULTURE,IVF/IVC)YDEFECUNDACIÓNPORINYECCIÓNINTRACITOPLASMÁTICA DEESPERMATOZOIDES/CULTIVO INTRAVAGINAL(INTRA-CYTOPLASMIC SPERMINJECTION/FERITILIZATION/INTRAVAGINAL
THE INTRAVAGINAL CULTURE SYSTEM INVOCELL™ CONSISTS OF THE FOLLOWING COMPONENTS: THE USE OF THE CULTURE SYSTEM IS INDICATED IN THE PREPARATION, RETENTION AND TRANSFER OF GAMETO-HUMAN EMBRYOS DURING THE PROCEDURES OF IN VITRO FERTILISATION/INTRAVAGINAL CULTURE IN VITRO (INVITROFERATION/INTRAVAGINAL CULTURE, IVF/IVC) AND FERTILISATION BY INTRACYTOPLASMIC SPERMINJECTION/FERITILISATION/INTRAVAGINAL