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Probes - ANVISA Registration 80475510013

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80475510013 and manufactured by Endosmart GmBH. The registration is held by E-MED PRODUTOS MÉDICO-HOSPITALARES 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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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80475510013
Registration Details
ANVISA Registration Number: 80475510013
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Device Details

Endosonda Nitinol Rígida
Risk Class II

Registration Details

80475510013

25351043629201527

03480968000150

Company Information

Endosmart GmBH
Germany
PT: ALEMANHA

Dates and Status

Feb 18, 2015

VIGENTE

09/18/2025 19:00:01