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Collection Vials - ANVISA Registration 80533420034

Access comprehensive regulatory information for Collection Vials in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80533420034 and manufactured by TONGLU QIANYAN MEDTECH CO. LTD.. The registration is held by ENDO-MASTER COMÉRCIO DE EQUIPAMENTOS OPTICOS E CIENTÍFICOS LTDA - EPP 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 3P MEDICAL LTDA, SEROPLAST INDÚSTRIA E COMÉRCIO DE PRODUTOS 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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80533420034
Registration Details
ANVISA Registration Number: 80533420034
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Device Details

Dreno de Sucção para Evacuador de Bexiga Descartável BottlePlus Endomaster
Risk Class II

Registration Details

80533420034

25351094982201709

05785287000126

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 17, 2017

VIGENTE

09/18/2025 19:00:01