Bone Densitometry Device - ANVISA Registration 80071260163

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 80071260163 and manufactured by manufacturer not specified. The registration is held by GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDA with validity until Jun 13, 2035.

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 OSTEOSYS CO., LTD, HOLOGIC, INC, 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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80071260163
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Registration Details
ANVISA Registration Number: 80071260163
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

DENSITOMETRO OSSEO LUNAR PRODIGY
Risk Class III

Registration Details

80071260163

25351090520201234

00029372000140

Dates and Status

Dec 10, 2012

13/06/2035

09/18/2025 19:00:01

DENSITOMETRO OSSEO LUNAR PRODIGY
Risk Class III

Registration Details

80071260163

25351090520201234

00029372000140

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 10, 2012

13/06/2035

09/18/2025 19:00:01

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