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Devices for Female Contraception - ANVISA Registration 80077400001

Access comprehensive regulatory information for Devices for Female Contraception in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80077400001 and manufactured by INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA. The registration is held by INJEFLEX INDÚSTRIA E COMÉRCIO DE DISPOSITIVOS E PRODUTOS MÉDICOS LTDA with validity until Jan 21, 2027.

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including SEMINA INDÚSTRIA E COMÉRCIO LTDA, SMB CORPORATION OF INDIA, 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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80077400001
Registration Details
ANVISA Registration Number: 80077400001
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Device Details

DISPOSITIVO INTRAUTERINO DE COBRE
Risk Class IV

Registration Details

80077400001

253510216680122

01997891000165

Dates and Status

Jan 21, 2002

21/01/2027

09/18/2025 19:00:01