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ICONIX SPEED - COFEPRIS Registration 1299C2018 SSA

Access comprehensive regulatory information for ICONIX SPEED (ICONIX SPEED) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1299C2018 SSA and manufactured by STRYKER Mร‰XICO, S.A. DE C.V.. The device was registered on June 01, 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.

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COFEPRIS Official Data
Clase III
1299C2018 SSA
ICONIX SPEED
COFEPRIS Analysis ID: 1299C2018 SSA
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Product Use / Uso del Producto
Spanish

LOS ANCLAJES ICONIX SPEED DE STRYKER SE HAN DISEร‘ADO PARA LA FIJACIร“N DE TEJIDOS BLANDOS AL HUESO EN EL HOMBRO. ESTรN INDICADOS PARA SU USO EN LA REPARACIร“N DEL MANGUITO DE LOS ROTADORES.

English

STRYKER'S ICONIX SPEED ANCHORS ARE DESIGNED FOR SOFT TISSUE ATTACHMENT TO BONE IN THE SHOULDER. THEY ARE INDICATED FOR USE IN ROTATOR CUFF REPAIR.

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)
ANCLAJES
Trade Name (English)
ANCHORS
Registration Information
Analysis ID
1299C2018 SSA
Registration Date
June 01, 2018
Manufacturer / Fabricante
Name (English)
STRYKER MEXICO, S.A. DE C.V.