PACKS STELLARIS ELITE™
Mexico·Clase II·I. MEDICAL EQUIPMENT·BAUSCH & LOMB MÉXICO, S.A. DE C.V.·Registered April 08, 2019LOS PACKS STELLARIS ELITE™ ESTÁN DISEÑADOS PARA SU USO CON LOS SISTEMAS MICROQUIRÚRGICOS PARA EL SEGMENTO ANTERIOR Y POSTERIOR DEL OJO PARA EL SISTEMA STELLARIS ELITE™ PARA LA FACOEMULSIFICACIÓN DEL CRISTALINO OPACIFICADO EN LA CIRUGÍA DEL SEGMENTO ANTERI
STELLARIS ELITE PACKS ARE DESIGNED FOR USE WITH MICROSURGICAL SYSTEMS FOR THE ANTERIOR AND POSTERIOR SEGMENT OF THE EYE FOR THE STELLARIS ELITE™™ SYSTEM FOR PHACOEMULSIFICATION OF THE OPACIFIED LENS IN ANTERI SEGMENT SURGERY
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- PAQUETES DE ACCESORIOS PARA EL SISTEMA MICROQUIRÚRGICO PARA EL SEGMENTO ANTERIOR Y POSTERIOR DEL OJO
- Trade Name (English)
- MICROSURGICAL SYSTEM ACCESSORY PACKAGES FOR THE ANTERIOR AND POSTERIOR SEGMENT OF THE EYE
- Analysis ID
- 716E2019 SSA
- Registration Date
- April 08, 2019
- Name (Spanish)
- BAUSCH & LOMB MÉXICO, S.A. DE C.V.
- Name (English)
- BAUSCH & LOMB MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for PACKS STELLARIS ELITE™ (PACKS STELLARIS ELITE™) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 716E2019 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on April 08, 2019.
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.