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ELECTRONIC AUTOINJECTOR FOR REBIF® - Cuba Medical Device Registration

Access comprehensive regulatory information for ELECTRONIC AUTOINJECTOR FOR REBIF® in the Cuba medical device market through Pure Global AI's free database. This NEUROLOGY medical device is manufactured by ARES TRADING SA, SWITZERLAND (ATSA). The device was registered on June 29, 2018.

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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Cuba CECMED Official Data
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NEUROLOGY
ELECTRONIC AUTOINJECTOR FOR REBIF®
AUTOINYECTOR ELECTRÓNICO PARA REBIF®
Cuba Medical Device Registration - CECMED
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Product Information
Description

REBISMART® 2.0

Product Use

ADMINISTRATION OF THE SOLUTION FOR INJECTION IN PRE-FILLED CARTRIDGES REBIF® NF 132MCG/1.5ML (44MCG/0.5ML)

ADMINISTRACIÓN DE LA SOLUCIÓN INYECTABLE EN CARTUCHOS PRE LLENADOS REBIF® NF 132MCG/1.5ML (44MCG/0.5ML)

Device Classification
Product Type
NEUROLOGY
NEUROLOGIA
Product Name
ELECTRONIC AUTOINJECTOR FOR REBIF®
AUTOINYECTOR ELECTRÓNICO PARA REBIF®
Registration Information
Registration Date
June 29, 2018
Expiration Date
June 29, 2023
Creation Date
March 23, 2023
Manufacturer
Name
ARES TRADING SA, SWITZERLAND (ATSA)
ARES TRADING SA, SUIZA (ATSA)