CLARITY ULTRA
Mexico·Clase I·IV. DENTAL SUPPLIES·3M MÉXICO, S.A. DE C.V.·Registered September 10, 2020BRACKETSUTILIZADOSENELTRATAMIENTODEORTODONCIA PARA CORREGIR LA ESTÉTICADENTAL DEL PACIENTE.
BRACKETS USED IN ORTHODONTIC TREATMENT TO CORRECT THE PATIENT'S DENTAL AESTHETICS.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- IV. INSUMOS DE USO ODONTOLÓGICO
- Product Type (English)
- IV. DENTAL SUPPLIES
- Trade Name (Spanish)
- SISTEMA DE BRACKETS DEAUTOLIGADO PASIVO
- Trade Name (English)
- PASSIVE SELF-LIGATING BRACKET SYSTEM
- Analysis ID
- 1219C2020 SSA
- Registration Date
- September 10, 2020
- Name (Spanish)
- 3M MÉXICO, S.A. DE C.V.
- Name (English)
- 3M MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for CLARITY ULTRA (CLARITY ULTRA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1219C2020 SSA and manufactured by 3M MÉXICO, S.A. DE C.V.. The device was registered on September 10, 2020.
This page provides complete registration details including product type (IV. DENTAL SUPPLIES), 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.