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

CORTISOL/CORTISONE - ANVISA Registration 10338930323

Access comprehensive regulatory information for CORTISOL/CORTISONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10338930323 and manufactured by IDS IMMUNODIAGNOSTIC SYSTEMS LTD.. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, DRG INSTRUMENTS GMBH, 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
10338930323
Registration Details
ANVISA Registration Number: 10338930323
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

FAMรLIA IDS-iSYS SALIVARY CORTISOL
Risk Class II

Registration Details

10338930323

25351374815202459

93741726000166

Company Information

England (United Kingdom)
PT: INGLATERRA (REINO UNIDO)

Dates and Status

Aug 26, 2024

VIGENTE

09/18/2025 19:00:01