U S C O P E
Mexico·Clase II·I. MEDICAL EQUIPMENT·MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.·Registered July 17, 2018"USCOPE HA SIDO DISEÑADO PARA SER USADO CON ACCESORIOS PARA ENDOTERAPIA TALES COMO FORCEPS PARA BIOPSIA Y OTROS EQUIPOS AUXILIARES PARA ENDOSCOPIA Y CIRUGÍA ENDOSCÓPICA DENTRO DEL TRACTO URINARIO Y EN EL INTERIOR DEL RIÑÓN. EL SISTEMA ES PARA USO EN HOSP
"USCOPE HAS BEEN DESIGNED TO BE USED WITH ENDOTHERAPY ACCESSORIES SUCH AS FORCEPS FOR BIOPSY AND OTHER AUXILIARY EQUIPMENT FOR ENDOSCOPY AND ENDOSCOPIC SURGERY WITHIN THE URINARY TRACT AND INSIDE THE KIDNEY. THE SYSTEM IS FOR USE IN HOSP
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- VIDEO ENDOSCOPIO MÉDICO
- Trade Name (English)
- VIDEO MEDICAL ENDOSCOPE
- Analysis ID
- 1750E2018 SSA
- Registration Date
- July 17, 2018
- Name (Spanish)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
- Name (English)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
Access comprehensive regulatory information for U S C O P E (U S C O P E) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1750E2018 SSA and manufactured by MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.. The device was registered on July 17, 2018.
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.