Pure Global AI
ANVISA registration 80337969003Active

Retinograph

ANVISA Registration Number: 80337969003TECNOVENT COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA MESHANGHAI MEDIWORKS PRECISION INSTRUMENT CO., LTD. (SANLU ROAD)Risk Class II
Device names
Technical name
Retinograph
PT: Retinografo
Commercial name
RETINOGRAFO DIGITAL BINOCULAR
Risk class
Class II
Registration details
Registration Number
80337969003
Process Number
25351030002202611
CNPJ
07912362000106
Company information
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Mar 16, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Retinograph in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80337969003 and manufactured by SHANGHAI MEDIWORKS PRECISION INSTRUMENT CO., LTD. (SANLU ROAD). The registration is held by TECNOVENT COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA ME with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.