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

IMMUNOHEMATOLOGY - RARE SERA FOR CONVENTIONAL METHODOLOGY - ANVISA Registration 80115310127

Access comprehensive regulatory information for IMMUNOHEMATOLOGY - RARE SERA FOR CONVENTIONAL METHODOLOGY in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80115310127 and manufactured by manufacturer not specified. The registration is held by KOVALENT DO BRASIL LTDA with validity until Aug 31, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MEDION GRIFOLS DIAGNOSTICS AG, MEDION DIAGNOSTICS GRIFOLS AG, 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
80115310127
2 Related Devices
Registration Details
ANVISA Registration Number: 80115310127
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Registration Details

80115310127

25351477862200833

04842199000156

Company Information

Dates and Status

Aug 31, 2009

31/08/2034

09/18/2025 19:00:01

Registration Details

80115310127

25351477862200833

04842199000156

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Aug 31, 2009

31/08/2034

09/18/2025 19:00:01