Devices For Urinary Incontinence - ANVISA Registration 80991380011

Access comprehensive regulatory information for Devices For Urinary Incontinence in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80991380011 and manufactured by KFF S.A. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO LTDA with validity until Jun 13, 2036.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including COOPER SURGICAL, INC., INDUSTRIA DE ARTEFATOS DE BORRACHA INOVATEX 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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80991380011
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Registration Details
ANVISA Registration Number: 80991380011
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

REDE POLIMÉRICA SLING INTERLIFT
Risk Class III

Registration Details

80991380011

25351140822201819

17634786000100

Company Information

KFF S.A
Argentina
PT: ARGENTINA

Dates and Status

Jun 18, 2018

13/06/2036

09/18/2025 19:00:01

REDE POLIMÉRICA SLING INTERLIFT
Risk Class III

Registration Details

80991380011

25351140822201819

17634786000100

Company Information

Dates and Status

Jun 18, 2018

13/06/2036

09/18/2025 19:00:01