Applicators - ANVISA Registration 80153820022

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80153820022 and manufactured by GUANGZHOU EKAI ELECTRONIC TECHNOLOGY CO. LTD. The registration is held by TG MED COMERCIO IMPORTACAO, EXPORTACAO, FABRICACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including FAGA MEDICAL INDUSTRIA DE EQUIPAMENTOS E INSTRUMENTOS MEDICO-HOSPITALARES LTDA ME, Baxter Healthcare S.A., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80153820022
Registration Details
ANVISA Registration Number: 80153820022
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

HYDRA PEN
Risk Class I

Registration Details

80153820022

25351350765202171

04058136000103

Company Information

Dates and Status

Apr 29, 2021

VIGENTE

09/18/2025 19:00:01