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

Probes - ANVISA Registration 10342319025

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10342319025 and manufactured by FLEXOR INDUSTRIA E COMERCIO DE PRODUTOS MEDICO HOSPITALAR LTDA. The registration is held by FLEXOR INDUSTRIA E COMERCIO DE PRODUTOS MEDICO HOSPITALAR 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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
10342319025
Registration Details
ANVISA Registration Number: 10342319025
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

SONDA GASTRICA ESPECIAL FOUCHET ESTERIL FLEXOR
Risk Class II

Registration Details

10342319025

25351180908202414

00947389000187

Company Information

Dates and Status

Apr 22, 2024

VIGENTE

09/18/2025 19:00:01