COBAN 2 - COFEPRIS Registration 290C2021 SSA
Access comprehensive regulatory information for COBAN 2 (COBAN 2) in the Mexico medical device market through Pure Global AI's free database. This Clase I-Bajo Riesgo medical device is registered under COFEPRIS analysis ID 290C2021 SSA and manufactured by 3M MÉXICO, S.A. DE C.V.. The device was registered on February 22, 2021.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
PARA PROPORCIONAR COMPRESIÓN PARAVARIOS DIAGNÓSTICOS MÉDICOS, TALESCOMO:LINFEDEMAYÚLCERASVENOSASENLASPIERNASYOTROSPROBLEMASCLÍNICOSQUEREQUIERENCOMPRESIÓN. ELSISTEMADE COMPRESIÓN COBAN 2 ESTÁRECOMENDADOPARASUUSOENPACIENTESCON UN ITB ≥ 0,8 Y SE UTILIZAPRINCIPALMENTEPARALAPIERNAYELPIE.ELSISTEMADECOMPRESIÓNCOBAN2LITEESTÁINDICADOPARASUUSOENPACIENTESCON UN ITB ≥ 0,5 Y SE UTILIZA ENEXTREMIDADES CON CIRCUNFERENCIASPEQUEÑAS. SE UTILIZA PRINCI
TO PROVIDE COMPRESSION FOR VARIOUS MEDICAL DIAGNOSES, SUCH AS:LYMPHEDEMA AND VENOUS LEG ULCERS AND OTHER CLINICAL PROBLEMS THAT REQUIRE COMPRESSION. THE COBAN 2 COMPRESSION SYSTEM IS RECOMMENDED FOR USE IN PATIENTS WITH A ≥ 0.8 AND IS MAINLY USED FOR THE LEG AND FOOT. THE COBAN2LITE COMPRESSION SYSTEM IS INDICATED FOR USE IN PATIENTS WITH A ≥ 0.5 AND IS USED IN LIMBS WITH SMALL CIRCUMFERENCES. MAIN USE