GONIOSCOPIO, MARCA NIDEK,MODELO: GS-1 - COFEPRIS Registration 42E2020 SSA
Access comprehensive regulatory information for GONIOSCOPIO, MARCA NIDEK,MODELO: GS-1 (GONIOSCOPY, BRAND NIDEK,MODEL: GS-1) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 42E2020 SSA and manufactured by S4OPTIK, S.A. DE C.V.. The device was registered on January 14, 2020.
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.
EL GONIOSCOPIO ES UN DISPOSITIVODISEÑADO PARA OBSERVAR, CAPTURAR OGRABAR IMÁGENES DEL OJO PARAPROPORCIONAR INFORMACIÓN DE IMÁGENESELECTRÓNICAS PARA EL DIAGNÓSTICO.
THE GONIOSCOPE IS A DEVICE DESIGNED TO OBSERVE, CAPTURE, OR RECORD IMAGES OF THE EYE TO PROVIDE ELECTRONIC IMAGING INFORMATION FOR DIAGNOSIS.