INVERTED NIPPLE CORRECTOR - ANVISA Registration 81319579002
Access comprehensive regulatory information for INVERTED NIPPLE CORRECTOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81319579002 and manufactured by LANSINOH LABORATORIES INC. The registration is held by LANSINOH DO BRASIL LABORATORIOS, IMPORTACAO E EXPORTACAO LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including PHILIPS CONSUMER LIFESTYLE BV, LANSINOH LABORATORIES INC, 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.
Device Details
Registration Details
81319579002
25351271969201627
20105196000196
Company Information
Dates and Status
Aug 29, 2016
VIGENTE
09/18/2025 19:00:01
CORRETOR DE MAMILOS INVERTIDOS
LATCH ASSISTยฎ CORRETOR DE MAMILOS
LANSINOH LABORATORIES INC
80116679001
Apr 08, 2013
CORRETOR DE MAMILOS INVERTIDOS
NIPLETTE
PHILIPS CONSUMER LIFESTYLE BV
10043669002
May 31, 2010

