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Intra-Uterine Devices - ANVISA Registration 80077400004

Access comprehensive regulatory information for Intra-Uterine Devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80077400004 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 Apr 14, 2028.

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including PREGNA INTERNATIONAL LIMITED, Meril Endo Surgery Pvt. 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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80077400004
Registration Details
ANVISA Registration Number: 80077400004
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Device Details

DISPOSITIVO INTRAUTERINO DE COBRE OPTIMA DIU ML CU 375
Risk Class IV

Registration Details

80077400004

25351632844200740

01997891000165

Dates and Status

Apr 14, 2008

14/04/2028

09/18/2025 19:00:01