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Tubes - ANVISA Registration 10341350838

Access comprehensive regulatory information for Tubes in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10341350838 and manufactured by XERIDIEM MEDICAL DEVICES, INC. The registration is held by BOSTON SCIENTIFIC DO BRASIL LTDA with validity until Oct 20, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including RICHARD WOLF GMBH, BIOVICO SP. Z 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.

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10341350838
2 Related Devices
Registration Details
ANVISA Registration Number: 10341350838
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Related Devices (2)

EndoVive™ Kit de Substituição de Balão Standard - Sonda Reta
Risk Class III

Registration Details

10341350838

25351758218201445

01513946000114

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 20, 2015

20/10/2035

09/18/2025 19:00:01

EndoVive™ Kit de Substituição de Balão Standard - Sonda Reta
Risk Class III

Registration Details

10341350838

25351758218201445

01513946000114

Company Information

Dates and Status

Oct 20, 2015

20/10/2035

09/18/2025 19:00:01