Software - ANVISA Registration 82507520001
Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82507520001 and manufactured by RESMED CORP.. The registration is held by RESMED BRASIL REPRESENTAÇÕES DE PRODUTOS MÉDICOS LTDA. with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., CARDIO SISTEMAS COMERCIAL E INDUSTRIAL LTDA, 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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Registration Details
82507520001
25351364417202262
07733293000165
Company Information
Dates and Status
Sep 29, 2022
VIGENTE
09/18/2025 19:00:01
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myAir
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AVIEW
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80488290040
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80147410026
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81806320006
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83126510001
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MV PEP
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80436840006
Sep 08, 2025
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Future Fertility Oocyte Software
FUTURE FERTILITY INC.
83084440002
Aug 18, 2025