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

PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 82531179006

Access comprehensive regulatory information for PERIPHERAL ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82531179006 and manufactured by POLYREY MEDICAL TECH(SUZHOU) CO., LTD. The registration is held by AQUINOSITE COMERCIO E SERVICOS LTDA-ME 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 BOSTON SCIENTIFIC CORPORATION, BROSMED MEDICAL 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
82531179006
Registration Details
ANVISA Registration Number: 82531179006
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

HYPERY CATETER BALÃO DE ALTA PRESSAO PARA ANGIOPLASTIA
Risk Class II

Registration Details

82531179006

25351081456202570

12259723000199

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 26, 2025

VIGENTE

09/18/2025 19:00:01