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Urethral Prostheses - ANVISA Registration 10306840126

Access comprehensive regulatory information for Urethral Prostheses in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10306840126 and manufactured by PROMEDON S.A. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until Jun 11, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including PROMEDON S.A, PROMEDON S.A., 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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10306840126
2 Related Devices
Registration Details
ANVISA Registration Number: 10306840126
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Related Devices (2)

IMPLANTE PARA TRATAMENTO DE PROLAPSO ANTERIOR CALISTAR A PROMEDON
Risk Class III

Registration Details

10306840126

25351094461201214

00028682000140

Company Information

PROMEDON S.A
Argentina
PT: ARGENTINA

Dates and Status

Jun 11, 2012

11/06/2027

09/18/2025 19:00:01

IMPLANTE PARA TRATAMENTO DE PROLAPSO ANTERIOR CALISTAR A PROMEDON
Risk Class III

Registration Details

10306840126

25351094461201214

00028682000140

Company Information

Dates and Status

Jun 11, 2012

11/06/2027

09/18/2025 19:00:01