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

Extension Tube - ANVISA Registration 80689090009

Access comprehensive regulatory information for Extension Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80689090009 and manufactured by SENORX INC.. The registration is held by BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA A SAÚDE 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 M P - COMERCIO E INDUSTRIA DE MATERIAIS HOSPITALARES LTDA, HARTMANN IND COM PRODS MEDICO HOSPITALARES LTDA, 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
80689090009
Registration Details
ANVISA Registration Number: 80689090009
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Extensão do Tubo de Vácuo Encor
Risk Class I

Registration Details

80689090009

25351469196201240

10818693000188

Company Information

SENORX INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 24, 2013

VIGENTE

09/18/2025 19:00:01