Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Infusion Pump - ANVISA Registration 80120790075

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 80120790075 and manufactured by manufacturer not specified. The registration is held by OPTIKA SISTEMAS PARA MEDICINA S/A with validity until Jun 18, 2028.

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80120790075
2 Related Devices
Registration Details
ANVISA Registration Number: 80120790075
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

BOMBA DE DRENAGEM CSF LIQUOGUARD 7
Risk Class III

Registration Details

80120790075

25351166953201818

04579646000126

Company Information

Dates and Status

Jun 18, 2018

18/06/2028

09/18/2025 19:00:01

BOMBA DE DRENAGEM CSF LIQUOGUARD 7
Risk Class III

Registration Details

80120790075

25351166953201818

04579646000126

Company Information

Germany
PT: ALEMANHA

Dates and Status

Jun 18, 2018

18/06/2028

09/18/2025 19:00:01