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RETINOSCOPIO BETA 200 - Cuba Medical Device Registration

Access comprehensive regulatory information for RETINOSCOPIO BETA 200 in the Cuba medical device market through Pure Global AI's free database. This OPHTHALMOLOGY medical device is manufactured by HEINE OPTOTECHNIK GMBH & CO. Medical history.. The device was registered on December 28, 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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OPHTHALMOLOGY
RETINOSCOPIO BETA 200
Cuba Medical Device Registration - CECMED
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Product Information
Description

C-034.23.420

Product Use

STUDY OF THE RETINA OF THE EYE

ESTUDIO DE LA RETINA DEL OJO

Device Classification
Product Type
OPHTHALMOLOGY
OFTALMOLOGIA
Product Name
RETINOSCOPIO BETA 200
Registration Information
Registration Date
December 28, 2018
Expiration Date
December 28, 2023
Creation Date
March 23, 2023
Manufacturer
Name
HEINE OPTOTECHNIK GMBH & CO. Medical history.
HEINE OPTOTECHNIK GMBH & CO.KG.