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Dilators - ANVISA Registration 80160409038

Access comprehensive regulatory information for Dilators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80160409038 and manufactured by HUNAN REBORN MEDICAL SCIENCE AND TECHNOLOGY DEVELOPMENT CO., LTD. The registration is held by ASHER-SILB MEDICAL DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MEDTEC SUPPLIES, INDUSTRIA, IMPORTACAO, EXPORTACAO, DISTRIBUICAO E COMERCIO LTDA, E-MED PRODUTOS Mร‰DICO-HOSPITALARES LTDA - ME, 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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80160409038
Registration Details
ANVISA Registration Number: 80160409038
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Device Details

Conjunto Dilatador Ureteral
Risk Class II

Registration Details

80160409038

25351067662202577

05353872000157

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

May 12, 2025

VIGENTE

09/18/2025 19:00:01