GONIOSCOPIO, MARCA NIDEK,MODELO: GS-1
Mexico·Clase II·I. MEDICAL EQUIPMENT·S4OPTIK, S.A. DE C.V.·Registered January 14, 2020EL 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.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- GONIOSCOPIO
- Trade Name (English)
- GONIOSCOPIO
- Analysis ID
- 42E2020 SSA
- Registration Date
- January 14, 2020
- Name (Spanish)
- S4OPTIK, S.A. DE C.V.
- Name (English)
- S4OPTIK, S.A. DE C.V.
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.