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

Laminar Flow System - ANVISA Registration 83019210001

Access comprehensive regulatory information for Laminar Flow System in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 83019210001 and manufactured by IVFTECH. The registration is held by E.M. ALBUQUERQUE 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 CONTROLAR INDÚSTRIA E COMÉRCIO DE FILTROS E EQUIPAMENTOS LTDA EPP, TELSTAR TECHNOLOGIES, S.L. (SOCIEDAD UNIPERSONAL), 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
83019210001
Registration Details
ANVISA Registration Number: 83019210001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

IV Ftech Sterica
Risk Class I

Registration Details

83019210001

25351093498202553

48653706000189

Company Information

IVFTECH
Denmark
PT: DINAMARCA

Dates and Status

Jul 07, 2025

VIGENTE

09/18/2025 19:00:01