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Tourniquet - ANVISA Registration 82099930002

Access comprehensive regulatory information for Tourniquet in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82099930002 and manufactured by ORTUS MEDI-TECH CO., LTD. The registration is held by SELLMED PRODUTOS MEDICOS E 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 SAFEGUARD MEDICAL TECHNOLOGIES LTD., WUXI EMSRUN TECHNOLOGY CO., LTD., 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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82099930002
Registration Details
ANVISA Registration Number: 82099930002
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Device Details

BANDAGEM DE PRESSÃO DESCARTÁVEL ANGIOTECH
Risk Class I

Registration Details

82099930002

25351412914202446

37438274000177

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 07, 2024

VIGENTE

09/18/2025 19:00:01