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DORNIER GEMINI - COFEPRIS Registration 1795E2018 SSA

Access comprehensive regulatory information for DORNIER GEMINI (DORNIER GEMINI) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1795E2018 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on July 24, 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.

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COFEPRIS Official Data
Clase II
1795E2018 SSA
DORNIER GEMINI
COFEPRIS Analysis ID: 1795E2018 SSA
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Product Use / Uso del Producto
Spanish

PARA LA FRAGMENTACIร“N DE LOS CรLCULOS DE LAS VรAS URINARIAS, ES DECIR CรLCULOS RENALES CALICIALES, CรCULOS RENALES Pร‰LVICOS Y CรLCULOS URETERALES.

English

FOR FRAGMENTATION OF URINARY TRACT STONES, I.E. GOBLET KIDNEY STONES, PELVIC KIDNEY STONES AND URETERAL STONES.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO Mร‰DICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
LITOTRIPTOR
Trade Name (English)
LITOTRIPTOR
Registration Information
Analysis ID
1795E2018 SSA
Registration Date
July 24, 2018
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL S.A. DE C.V.