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Instrument Kit - ANVISA Registration 80005439068

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 80005439068 and manufactured by WRIGHT MEDICAL TECHNOLOGY, INC (MEMPHIS). The registration is held by STRYKER DO BRASIL 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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80005439068
Registration Details
ANVISA Registration Number: 80005439068
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Device Details

Kit Instrumental Prostep MIS MICA SOLO Guide
Risk Class II

Registration Details

80005439068

25351415712202456

02966317000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Oct 14, 2024

VIGENTE

09/18/2025 19:00:01