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DIASAFE® PLUS FILTER HAEMODIALYSIS MACHINE - Cuba Medical Device Registration

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.

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NEPHROLOGY
DIASAFE® PLUS FILTER HAEMODIALYSIS MACHINE
MÁQUINA DE HEMODIÁLISIS CON FILTRO DIASAFE® PLUS
Cuba Medical Device Registration - CECMED
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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

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