HEALON DUET PRO
Mexico·Clase III·V. SURGICAL AND HEALING MATERIALS·JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.·Registered September 13, 2019ESTÁ DISEÑADO PARA PROPORCIONAR DOS PRODUCTOS VISCOELÁSTICOS CON CARACTERÍSTICAS FISIOQUÍMICAS DIFERENTES QUE PUEDEN UTILIZARSE COMBINADOS PARA REALIZAR TAREAS ESPECÍFICAS DURANTE LA INTERVENCIÓN QUIRÚRGICA DE CATARATAS. PARA CIRUGÍA OCULAR. EN PROCEDIMIE
IT IS DESIGNED TO PROVIDE TWO VISCOELASTIC PRODUCTS WITH DIFFERENT PHYSIOCHEMICAL CHARACTERISTICS THAT CAN BE USED IN COMBINATION TO PERFORM SPECIFIC TASKS DURING CATARACT SURGERY. FOR EYE SURGERY. IN PROCEDURE
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
- Product Type (English)
- V. SURGICAL AND HEALING MATERIALS
- Trade Name (Spanish)
- DISPOSITIVO VISCOQUIRÚRGICO OFTÁLMICO
- Trade Name (English)
- OPHTHALMIC VISCOSURGICAL DEVICE
- Analysis ID
- 1865C2019 SSA
- Registration Date
- September 13, 2019
- Name (Spanish)
- JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.
- Name (English)
- JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for HEALON DUET PRO (HEALON DUET PRO) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1865C2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on September 13, 2019.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.