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Catheter Dilator - ANVISA Registration 82702709019

Access comprehensive regulatory information for Catheter Dilator in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82702709019 and manufactured by ENDO AMÉRICAS INDÚSTRIA E COMÉRCIO DE MATERIAL MÉDICO HOSPITALAR LTDA. The registration is held by ENDO AMÉRICAS INDÚSTRIA E COMÉRCIO DE MATERIAL MÉDICO HOSPITALAR 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 BROSMED MEDICAL CO., LTD, BRUN MEDICAL CO., LTD, 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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82702709019
Registration Details
ANVISA Registration Number: 82702709019
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Device Details

Kit Cânula MiniPerck Aspira
Risk Class II

Registration Details

82702709019

25351422161202487

37927322000190

Dates and Status

Nov 04, 2024

VIGENTE

09/18/2025 19:00:01