Pure Global

Craniotomes - ANVISA Registration 81125219001

Access comprehensive regulatory information for Craniotomes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81125219001 and manufactured by G C DE ALMEIDA E CIA LTDA - ME. The registration is held by G C DE ALMEIDA E CIA LTDA - ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including CODMAN & SHURTLEFF INC, MEDOS SARL, and 4 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
3 Competitors
4 Recent Registrations
81125219001
Registration Details
ANVISA Registration Number: 81125219001
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

CRANIร“TOMO DRILL PNEUMรTICO MAARTEC
Risk Class II

Registration Details

81125219001

25351005526201570

11480646000130

Company Information

Brazil
PT: BRASIL

Dates and Status

Apr 20, 2015

VIGENTE

09/18/2025 19:00:01