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Instrument Kit - ANVISA Registration 80733590011

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80733590011 and manufactured by DLR MEDIKAL SAN. VE DIS. TIC. LTD. STI. The registration is held by ANSER-BR COMERCIO DE PRODUTOS PARA SAUDE LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 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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80733590011
Registration Details
ANVISA Registration Number: 80733590011
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Device Details

Kit Dilatador Amplatz
Risk Class II

Registration Details

80733590011

25351109955201991

11825879000127

Company Information

Turkey
PT: TURQUIA

Dates and Status

Sep 30, 2019

VIGENTE

09/18/2025 19:00:01