ANAL IMPLANT - ANVISA Registration 10306840111
Access comprehensive regulatory information for ANAL IMPLANT in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10306840111 and manufactured by manufacturer not specified. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until Mar 29, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including PROMEDON S.A, and 2 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
10306840111
25351010437200908
00028682000140
Company Information
Dates and Status
Mar 29, 2010
29/03/2035
09/18/2025 19:00:01
ANAL IMPLANT
ANPHIS MICROSLING PARA INCONTINÊNCIA FECAL
PROMEDON S.A
10306840119
Apr 25, 2011
ANAL IMPLANT
ANPHIS MICROSLING PARA INCONTINÊNCIA FECAL
Not specified
10306840119
Apr 25, 2011
Devices
PERISTEEN PLUG ANAL
COLOPLAST A/S
10430310035
Jan 02, 2006
IMPLANTABLE SURGICAL MESH
EXIA
PROMEDON S.A.
10306840189
Jan 11, 2021
IMPLANTABLE SURGICAL MESH
EXIA
Not specified
10306840189
Jan 11, 2021