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Infusion Pump - ANVISA Registration 80145110159

Access comprehensive regulatory information for Infusion Pump in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80145110159 and manufactured by FRESENIUS VIAL. The registration is held by FRESENIUS KABI BRASIL LTDA with validity until Mar 26, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SHENZHEN COMEN MEDICAL INSTRUMENTS CO., LTD., LIFEMED INDUSTRIAL DE EQUIPAMENTOS E ARTiGOS Mร‰DICOS E HOSPITALARES 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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80145110159
2 Related Devices
Registration Details
ANVISA Registration Number: 80145110159
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Related Devices (2)

BOMBA DE SERINGA INJECTOMAT AGILIA
Risk Class III

Registration Details

80145110159

25351157761200687

49324221000104

Company Information

FRESENIUS VIAL
France
PT: FRANร‡A

Dates and Status

Mar 26, 2007

26/03/2027

09/18/2025 19:00:01

BOMBA DE SERINGA INJECTOMAT AGILIA
Risk Class III

Registration Details

80145110159

25351157761200687

49324221000104

Company Information

Dates and Status

Mar 26, 2007

26/03/2027

09/18/2025 19:00:01