INVERTED NIPPLE CORRECTOR - ANVISA Registration 80116679001
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 80116679001 and manufactured by LANSINOH LABORATORIES INC. The registration is held by PROIMPORT BRASIL S.A. with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

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Registration Details
80116679001
25351720904201284
03861474000116
Company Information
Dates and Status
Apr 08, 2013
VIGENTE
09/18/2025 19:00:01
INVERTED NIPPLE CORRECTOR
Lansinoh LatchAssist
LANSINOH LABORATORIES INC
81319579002
Aug 29, 2016
INVERTED NIPPLE CORRECTOR
NIPLETTE
PHILIPS CONSUMER LIFESTYLE BV
10043669002
May 31, 2010
Patient Immobilization Support
POSICIONADOR DE MAMA - MOD. PMAC
MEDINTEC LATIN AMERICA LTDA EPP
80186829007
Feb 26, 2018
Positioning Support
BreastStep
IT-V Medizintechnik GmbH
80569320023
May 17, 2017
Post-Surgical Mesh
Modelador Pós Cirúrgico
DRA CINTAS E MODELADORES LTDA
82773550005
Dec 16, 2024