{"id":1121,"date":"2022-03-16T23:29:15","date_gmt":"2022-03-16T23:29:15","guid":{"rendered":"https:\/\/pharmacare.cl\/?p=1121"},"modified":"2022-04-01T04:05:05","modified_gmt":"2022-04-01T04:05:05","slug":"dispositivos-medicos","status":"publish","type":"post","link":"https:\/\/pharmacare.cl\/?p=1121","title":{"rendered":""},"content":{"rendered":"

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Documentos de inter\u00e9s – Dispositivos M\u00e9dicos<\/h3>\n

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– Decreto 825 – APRUEBA REGLAMENTO DE CONTROL DE PRODUCTOS Y ELEMENTOS DE USO MEDICO – 21 AGOSTO 1999<\/a><\/p>\n

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– GUIA PARA LA CLASIFICACION DE DM SEGUN RIESGO – JUNIO 2018<\/a><\/p>\n

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– PROTOCOLO VERIFICACION KITS – 29 OCTUBRE 2020<\/a><\/p>\n

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