Modular stem for hip arthroplasty - ANVISA Registration 81202190012
Access comprehensive regulatory information for Modular stem for hip arthroplasty in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81202190012 and manufactured by ORTOSINTESE INDÚSTRIA E COMÉRCIO LTDA. The registration is held by ORTOSINTESE INDÚSTRIA E COMÉRCIO LTDA with validity until Jan 27, 2030.
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ZIMMER, INC., GROUPE LÉPINE, 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.
Device Details
Registration Details
81202190012
25351326304201711
48240709000352
Company Information
Dates and Status
Jan 27, 2020
27/01/2030
09/18/2025 19:00:01
Haste modular para artroplastia de quadril
Haste Femoral Não Cimentada Actis DuoFix
DEPUY IRELAND UC
80145901865
Feb 26, 2018
Haste modular para artroplastia de quadril
Haste Femoral Não Cimentada Actis DuoFix
DEPUY (IRELAND)
80145901865
Feb 26, 2018
Haste modular para artroplastia de quadril
Haste Femoral Não Cimentada Actis DuoFix
Not specified
80145901865
Feb 26, 2018
Haste modular para artroplastia de quadril
HASTES FEMORAIS MODULARES ZMR
ZIMMER, INC.
80044680318
Oct 16, 2017
Haste modular para artroplastia de quadril
HASTES FEMORAIS MODULARES ZMR
Not specified
80044680318
Oct 16, 2017

