KIT DE ACCESORIOS PARATALADRO CAYENNE.
Mexico·Clase I·I. MEDICAL EQUIPMENT·BIOMET MÉXICO, S.A. DE C.V.·Registered October 15, 2020EL KIT DE ACCESORIOS PARA TALADROCAYENNE ESTÁ INDICADO PARA USARSE ENPROCEDIMIENTOS QUIRÚRGICOS ASOCIADOSCON TENODESIS Y OTRAS INTERVENCIONESQUIRÚRGICAS ORTOPÉDICAS. PARAUTILIZARSE UNA SOLA VEZ, EN UN SOLOPACIENTE. NOREUTILIZAR,NIRE-ESTÉRILIZARBAJO NINGUNA CIRCUNSTANCIA.
THE DRILL CAYENNE ACCESSORY KIT IS INDICATED FOR USE IN SURGICAL PROCEDURES ASSOCIATED WITH TENODESIS AND OTHER ORTHOPEDIC SURGICAL INTERVENTIONS. TO BE USED ONLY ONCE, IN A SINGLE PATIENT. DO NOT REUSE, NIRE-STERILIZE UNDER ANY CIRCUMSTANCES.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- ACCESORIOSPARALAPERFORACIÓNDE CAVIDADES Y TÚNELES ÓSEOS.
- Trade Name (English)
- ACCESSORIES FOR THE PERFORATION OF CAVITIES AND BONE TUNNELS.
- Analysis ID
- 1421E2020 SSA
- Registration Date
- October 15, 2020
- Name (Spanish)
- BIOMET MÉXICO, S.A. DE C.V.
- Name (English)
- BIOMET MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for KIT DE ACCESORIOS PARATALADRO CAYENNE. (ACCESSORY KIT FOR CAYENNE DRILL.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1421E2020 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on October 15, 2020.
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.