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

COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III - ANVISA Registration 80615950232

Access comprehensive regulatory information for COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80615950232 and manufactured by HUMASIS CO., LTDA. The registration is held by Diagmaster Científica ltda with validity until Aug 19, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BIO-RAD LABORATORIES INC, RADIOMETER MEDICAL APS, 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
80615950232
2 Related Devices
Registration Details
ANVISA Registration Number: 80615950232
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Registration Details

80615950232

25351448450201949

09322796000173

Company Information

HUMASIS CO., LTDA
South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 19, 2019

19/08/2029

09/18/2025 19:00:01

Registration Details

80615950232

25351448450201949

09322796000173

Company Information

Dates and Status

Aug 19, 2019

19/08/2029

09/18/2025 19:00:01