LEISHMANIA SP - ANVISA Registration 10259610214

Access comprehensive regulatory information for LEISHMANIA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10259610214 and manufactured by VIRCELL S.L.. The registration is held by MEDIVAX INDÚSTRIA E COMÉRCIO LTDA with validity until Sep 21, 2025.

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 ADVAGEN BIOTECH LTDA, QUIBASA QUÍMICA BÁSICA LTDA, 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
10259610214
2 Related Devices
Registration Details
ANVISA Registration Number: 10259610214
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)

LEISHMANIA ELISA IgG+IgM
Risk Class III
Expired

Registration Details

10259610214

25351142474202373

68814961000173

Company Information

VIRCELL S.L.
Spain
PT: ESPANHA

Dates and Status

Mar 27, 2023

21/09/2025

09/18/2025 19:00:01

LEISHMANIA ELISA IgG+IgM
Risk Class III
Expired

Registration Details

10259610214

25351142474202373

68814961000173

Company Information

Dates and Status

Mar 27, 2023

21/09/2025

09/18/2025 19:00:01