Pure Global

ADRENOCORTICOTROPIC HORMONE (ACTH) - ANVISA Registration 82378830041

Access comprehensive regulatory information for ADRENOCORTICOTROPIC HORMONE (ACTH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82378830041 and manufactured by DIRUI INDUSTRIAL CO. LTD. The registration is held by CHINA MEHECO BRASIL COMERCIO E DISTRIBUICAO DE EQUIPAMENTOS E MATERIAIS MEDICOS 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, DIASORIN ITALIA S.P.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
82378830041
Registration Details
ANVISA Registration Number: 82378830041
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

KIT DE DETECÇÃO DE HORMÔNIO ADRENOCORTICOTRÓFICO (ACTH) - DIRUI
Risk Class II

Registration Details

82378830041

25351846458202353

37338619000110

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 02, 2024

VIGENTE

09/18/2025 19:00:01