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Applicators - ANVISA Registration 81398250010

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81398250010 and manufactured by CRYOLIFE, INC. The registration is held by Jotec do Brasil importação e comercio de equipamentos 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 FAGA MEDICAL INDUSTRIA DE EQUIPAMENTOS E INSTRUMENTOS MEDICO-HOSPITALARES LTDA ME, Baxter Healthcare S.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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81398250010
Registration Details
ANVISA Registration Number: 81398250010
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Device Details

Ponta Espátula Aplicadora Bioglue
Risk Class II

Registration Details

81398250010

25351638081201984

21996505000128

Company Information

CRYOLIFE, INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 09, 2019

VIGENTE

09/18/2025 19:00:01