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EM SA IMPLANT - COFEPRIS Registration 1882C2021 SSA

Access comprehensive regulatory information for EM SA IMPLANT (EM SA IMPLANT) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1882C2021 SSA and manufactured by HIOSSEN DE Mร‰XICO,S.A. DE C.V.. The device was registered on November 19, 2021.

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.

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COFEPRIS Official Data
Clase III
1882C2021 SSA
EM SA IMPLANT
COFEPRIS Analysis ID: 1882C2021 SSA
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Product Use / Uso del Producto
Spanish

ELIMPLANTEEMSA(CRESTAESTRECHA)ESTรDESTINADO PARA USARSE EN ELTRATAMIENTODEINCISIVOSMANDIBULARESCENTRALES Y LATERALES FALTANTES PARASOPORTAR DISPOSITIVOS PROTร‰SICOS

English

THE EMSA IMPLANT (NARROW RIDGE) IS INTENDED FOR USE IN THE TREATMENT OF MISSING CENTRAL AND LATERAL MANDIBULAR INCISIVES TO SUPPORT PROSTHETIC DEVICES

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ร“RTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
IMPLANTE DENTAL ENDOร“SEO
Trade Name (English)
ENDOOSSEOUS DENTAL IMPLANT
Registration Information
Analysis ID
1882C2021 SSA
Registration Date
November 19, 2021
Manufacturer / Fabricante
Name (English)
HIOSSEN DE Mร‰XICO,S.A. DE C.V.