Pure Global AI
ANVISA registration 80475510279Active

Retoscópio

ANVISA Registration Number: 80475510279E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - MEE-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - MERisk Class I
Verified
Device names
Technical name
Retoscópio
View exact technical-name matches →
Commercial name
Retoscópio Mendes
View exact commercial-name matches →
Risk class
Class I
Registration details
Registration Number
80475510279
Process Number
25351076348202666
CNPJ
03480968000150
Company information
Registration Holder
E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME
Manufacturer
E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
May 25, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Retoscópio in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80475510279 and manufactured by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME. The registration is held by E-MED PRODUTOS MÉDICO-HOSPITALARES 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.