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Intra-Uterine Devices - ANVISA Registration 10208250037

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 10208250037 and manufactured by manufacturer not specified. The registration is held by DKT DO BRASIL PRODUTOS DE USO PESSOAL LTDA with validity until Feb 22, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 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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10208250037
2 Related Devices
Registration Details
ANVISA Registration Number: 10208250037
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Related Devices (2)

ANDALAN SILVERFLEX
Risk Class IV

Registration Details

10208250037

25351206308201538

38756680000140

Company Information

Dates and Status

Feb 22, 2016

22/02/2026

09/18/2025 19:00:01

ANDALAN SILVERFLEX
Risk Class IV

Registration Details

10208250037

25351206308201538

38756680000140

Company Information

India
PT: รNDIA

Dates and Status

Feb 22, 2016

22/02/2026

09/18/2025 19:00:01