CONJUNTO DE MUÑÓN UNIVERSAL NEODENT
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·MANOHAY MÉXICO, S.A DE C.V.·Registered March 07, 2018CONJUNTO DE INSTRUMENTOS USADOS EN LA PRÓTESIS DE IMPLANTE SOPORTADAS, PLANEADAS DE ACUERDO CON CADA CASO, MANTENIENDO LA FUNCIÓN Y ESTÉTICA.
SET OF INSTRUMENTS USED IN THE IMPLANT PROSTHESIS SUPPORTED, PLANNED ACCORDING TO EACH CASE, MAINTAINING THE FUNCTION AND AESTHETICS.
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- COMPONENTES DE IMPLANTE ODONTOLÓGICO
- Trade Name (English)
- DENTAL IMPLANT COMPONENTS
- Analysis ID
- 694C2018 SSA
- Registration Date
- March 07, 2018
- Name (Spanish)
- MANOHAY MÉXICO, S.A DE C.V.
- Name (English)
- MANOHAY MÉXICO, S.A DE C.V.
Access comprehensive regulatory information for CONJUNTO DE MUÑÓN UNIVERSAL NEODENT (NEODENT UNIVERSAL RESIDUAL LIMB ASSEMBLY) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 694C2018 SSA and manufactured by MANOHAY MÉXICO, S.A DE C.V.. The device was registered on March 07, 2018.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.