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Surgical Kit - ANVISA Registration 82603649027

Access comprehensive regulatory information for Surgical 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 82603649027 and manufactured by MEDFACTOR INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDA. The registration is held by MEDFACTOR INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES 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, Humanna Medical Ltda, 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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82603649027
Registration Details
ANVISA Registration Number: 82603649027
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Device Details

Kit EndoDisc PurePrecision O.I.
Risk Class II

Registration Details

82603649027

25351149150202528

42313325000174

Dates and Status

Sep 08, 2025

VIGENTE

09/18/2025 19:00:01