CECMED registration

DIASAFE® PLUS FILTER HAEMODIALYSIS MACHINE

MÁQUINA DE HEMODIÁLISIS CON FILTRO DIASAFE® PLUS

FRESENIUS MEDICAL CARE AG & CO. KGAA.·NEPHROLOGY·Cuba CECMED·Registered May 30, 2023

Device classification

Product type: NEPHROLOGY
NEFROLOGIA
Product name: DIASAFE® PLUS FILTER HAEMODIALYSIS MACHINE
MÁQUINA DE HEMODIÁLISIS CON FILTRO DIASAFE® PLUS

Registration information

Registration date: May 30, 2023
Expiration date: May 30, 2028
Creation date: March 23, 2023

Manufacturer

Name: FRESENIUS MEDICAL CARE AG & CO. KGAA.

Product information

Description

4008S WITH SOFTWARE VERSION 12.0.

4008S CON VERSIÓN DE SOFTWARE 12.0.

Product use

HAEMODIALYSIS TREATMENT OF PATIENTS WITH ACUTE OR CHRONIC RENAL FAILURE

TRATAMIENTO DE HEMODIÁLISIS DE PACIENTES CON FALLO RENAL AGUDO O CRÓNICO

About this record

Access comprehensive regulatory information for DIASAFE® PLUS FILTER HAEMODIALYSIS MACHINE in the Cuba medical device market through Pure Global AI's free database. This NEPHROLOGY medical device is manufactured by FRESENIUS MEDICAL CARE AG & CO. KGAA.. The device was registered on May 30, 2023.

This page provides complete registration details including product information, product use, manufacturer details, and regulatory compliance data from the official Cuba CECMED medical device database. Pure Global AI offers free access to Cuba's medical device registry with bilingual Spanish/English content, helping global MedTech companies navigate Cuba regulations efficiently.