Instrument Kit - ANVISA Registration 80136990715
Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80136990715 and manufactured by AESCULAP AG. The registration is held by LABORATORIOS B. BRAUN 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, 5 companies making the same product including MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.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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Registration Details
80136990715
25351144077201202
31673254000102
Company Information
Dates and Status
Apr 30, 2012
VIGENTE
09/18/2025 19:00:01
Instrument Kit
INSTRUMENTAL PARA O SISTEMA COLUMBUS REVISÃO
AESCULAP AG
80136990659
Apr 19, 2010
Instrument Kit
Instrumentais Persona Revision
ZIMMER, INC
80044689033
Aug 05, 2021
Instrument Kit
INSTRUMENTAL BICONTACT REVISÃO
AESCULAP AG
80136990610
Jul 27, 2009
Instrument Kit
Instrumentais ATTUNE REVISION
DEPUY ORTHOPAEDICS INC
80145901892
Jan 21, 2019
Instrument Kit
Instrumentais ATTUNE REVISION
DEPUY (IRELAND)
80145901892
Jan 21, 2019
MARDEN MEDICAL LTDA• Brazil
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ICONACY ORTHOPEDIC IMPLANTS INDUSTRIA E COMERCIO DE PRODUTOS MEDICO HOSPITALARES LTDA• Brazil
E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME• Brazil
S.I.N. IMPLANT SYSTEM LTDA• Brazil
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