Pure Global

Probes - ANVISA Registration 10297020075

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 10297020075 and manufactured by Electroplast S/A. The registration is held by BADEIA COMERCIO IMPORTAÇÃO 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
10297020075
Registration Details
ANVISA Registration Number: 10297020075
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

SONDA/TUBO ENDOTRAQUEAL COM BALÃO, BCI MEDICAL
Risk Class II

Registration Details

10297020075

25351001035201168

43566371000148

Company Information

Electroplast S/A
Uruguay
PT: URUGUAI

Dates and Status

Apr 25, 2011

VIGENTE

09/18/2025 19:00:01