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

Tracheal Tube - ANVISA Registration 82059269013

Access comprehensive regulatory information for Tracheal Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82059269013 and manufactured by NINGBO MFLAB MEDICAL INSTRUMENTS CO., LTD. The registration is held by DLM 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 ZHANJIANG STAR ENTERPRISE CO,.LTD, HANGZHOU FORMED MEDICAL DEVICES CO., LTD, 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
82059269013
Registration Details
ANVISA Registration Number: 82059269013
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Sonda Endotraqueal Sem Balรฃo DLM
Risk Class II

Registration Details

82059269013

25351147608202261

34186181000104

Company Information

China
PT: CHINA, REPรšBLICA POPULAR

Dates and Status

Jul 07, 2022

VIGENTE

09/18/2025 19:00:01