Pure Global

INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 80012280215

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80012280215 and manufactured by manufacturer not specified. The registration is held by TERUMO MEDICAL DO BRASIL LTDA. with validity until Aug 01, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, TERUMO CORPORATION, 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
80012280215
2 Related Devices
Registration Details
ANVISA Registration Number: 80012280215
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Related Devices (2)

Radifocus Glidecath โ€“ Cateter Angiogrรกfico Terumo
Risk Class IV

Registration Details

80012280215

25351150722202279

03129105000133

Company Information

Dates and Status

Aug 01, 2022

01/08/2032

09/18/2025 19:00:01

Radifocus Glidecath โ€“ Cateter Angiogrรกfico Terumo
Risk Class IV

Registration Details

80012280215

25351150722202279

03129105000133

Company Information

TERUMO CORPORATION
Japan
PT: JAPรƒO

Dates and Status

Aug 01, 2022

01/08/2032

09/18/2025 19:00:01