YELLOW FEVER - ANVISA Registration 10330660287

Access comprehensive regulatory information for YELLOW FEVER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10330660287 and manufactured by SD BIOSENSOR INC.. The registration is held by DESCARPACK DESCARTAVEIS DO BRASIL LTDA with validity until Mar 02, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMA, INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ, 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 Similar Products
5 Competitors
10330660287
2 Related Devices
Registration Details
ANVISA Registration Number: 10330660287
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

Teste Rápido Standard Q Febre Amarela IgM
Risk Class III

Registration Details

10330660287

25351696314201963

01057428000133

Company Information

SD BIOSENSOR INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Mar 02, 2020

02/03/2030

09/18/2025 19:00:01

Teste Rápido Standard Q Febre Amarela IgM
Risk Class III

Registration Details

10330660287

25351696314201963

01057428000133

Company Information

Dates and Status

Mar 02, 2020

02/03/2030

09/18/2025 19:00:01