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Kit for venous/arterial catheter - ANVISA Registration 80991380021

Access comprehensive regulatory information for Kit for venous/arterial catheter in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80991380021 and manufactured by manufacturer not specified. The registration is held by DR IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO LTDA with validity until May 17, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including HEALTH QUALITY - INDUSTRIA E COMERCIO LTDA, SHAOXING HAITECH MEDICAL PRODUCTS 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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80991380021
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Registration Details
ANVISA Registration Number: 80991380021
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Related Devices (2)

KIT CATETER PARA HEMODIÁLISE E PLASMAFERESE DE LONGA PERMANÊNCIA INNOVA
Risk Class III

Registration Details

80991380021

25351644881201934

17634786000100

Company Information

Dates and Status

Dec 02, 2019

17/05/2035

09/18/2025 19:00:01

KIT CATETER PARA HEMODIÁLISE E PLASMAFERESE DE LONGA PERMANÊNCIA INNOVA
Risk Class III

Registration Details

80991380021

25351644881201934

17634786000100

Company Information

KFF S.A
Argentina
PT: ARGENTINA

Dates and Status

Dec 02, 2019

17/05/2035

09/18/2025 19:00:01