Pure Global

Biopsy Device - ANVISA Registration 81504799179

Access comprehensive regulatory information for Biopsy Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81504799179 and manufactured by ZHEJIANG CHUANGXIANG MEDICAL TECHNOLOGY CO., LTD.. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME 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 STERYLAB S.R.L., Zamar D.O.O., 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81504799179
Registration Details
ANVISA Registration Number: 81504799179
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Cesto de recuperação de uso único
Risk Class II

Registration Details

81504799179

25351021150202564

26185222000110

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Feb 24, 2025

VIGENTE

09/18/2025 19:00:01