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

INSTRUMENT (WITHOUT USE OF REAGENTS) - ANVISA Registration 80279429012

Access comprehensive regulatory information for INSTRUMENT (WITHOUT USE OF REAGENTS) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80279429012 and manufactured by CIRCASSIA AB. The registration is held by FORMED - COMERCIO DE PRODUTOS MEDICOS E COSMETICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including SHENZHEN ZHONGHE HEADWAY BIO-SCI & TECH CO., LTD., GERATHERM MEDICAL LATIN AMERICA LTDA., and 4 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
3 Competitors
4 Recent Registrations
80279429012
Registration Details
ANVISA Registration Number: 80279429012
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

80279429012

25351576480201944

07139218000170

Company Information

CIRCASSIA AB
Sweden
PT: SUร‰CIA

Dates and Status

Oct 29, 2019

VIGENTE

09/18/2025 19:00:01