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Instrument Kit - ANVISA Registration 81365089008

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 81365089008 and manufactured by MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES (MIDLABS INC.). The registration is held by vertek consumo clinico e hospitalar Ltda me 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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81365089008
Registration Details
ANVISA Registration Number: 81365089008
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Device Details

Cร‚NULA DE INSERร‡รƒO
Risk Class II

Registration Details

81365089008

25351149912202596

22898875000195

Company Information

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

Dates and Status

Sep 08, 2025

VIGENTE

09/18/2025 19:00:01