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

RADIOPAQUE MARKER - ANVISA Registration 80689090192

Access comprehensive regulatory information for RADIOPAQUE MARKER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80689090192 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The registration is held by BARD BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA A SAÚDE LTDA. with validity until Jan 03, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including REACT TECHNOLOGY INDUSTRIA COMERCIO IMPORTACAO E EXPORTACAO DE PRODUTOS MEDICOS E HOSPITALARES LTDA, BARD PERIPHERAL VASCULAR, INC., 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
80689090192
2 Related Devices
Registration Details
ANVISA Registration Number: 80689090192
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

UltraCor Twirl
Risk Class III

Registration Details

80689090192

25351247686202184

10818693000188

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 03, 2022

03/01/2032

09/18/2025 19:00:01

UltraCor Twirl
Risk Class III

Registration Details

80689090192

25351247686202184

10818693000188

Dates and Status

Jan 03, 2022

03/01/2032

09/18/2025 19:00:01