Infusion Pump - ANVISA Registration 80145110240

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 80145110240 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS KABI BRASIL LTDA with validity until Feb 05, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SHENZHEN COMEN MEDICAL INSTRUMENTS CO., LTD., LIFEMED INDUSTRIAL DE EQUIPAMENTOS E ARTiGOS MÉDICOS 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80145110240
2 Related Devices
Registration Details
ANVISA Registration Number: 80145110240
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

Família de Bombas Agilia SP
Risk Class III

Registration Details

80145110240

25351614564201721

49324221000104

Company Information

FRESENIUS KABI AG
Germany
PT: ALEMANHA

Dates and Status

Feb 05, 2018

05/02/2028

09/18/2025 19:00:01

Família de Bombas Agilia SP
Risk Class III

Registration Details

80145110240

25351614564201721

49324221000104

Company Information

Dates and Status

Feb 05, 2018

05/02/2028

09/18/2025 19:00:01