Bone Densitometry Device - ANVISA Registration 81504790224

Access comprehensive regulatory information for Bone Densitometry Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81504790224 and manufactured by HOLOGIC, INC. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME with validity until Aug 10, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including GE MEDICAL SYSTEMS ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC, OSTEOSYS CO., LTD, and 4 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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81504790224
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Registration Details
ANVISA Registration Number: 81504790224
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

DESINTÔMETRO ÓSSEO DE RAIO X QDR
Risk Class III

Registration Details

81504790224

25351763520202020

26185222000110

Company Information

HOLOGIC, INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 10, 2020

10/08/2030

09/18/2025 19:00:01

DESINTÔMETRO ÓSSEO DE RAIO X QDR
Risk Class III

Registration Details

81504790224

25351763520202020

26185222000110

Dates and Status

Aug 10, 2020

10/08/2030

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "Bone Densitometry Device"