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

CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 10407990081

Access comprehensive regulatory information for CORONARY ANGIOPLASTY BALLOON 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 10407990081 and manufactured by manufacturer not specified. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO LTDA with validity until Jan 06, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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
10407990081
2 Related Devices
Registration Details
ANVISA Registration Number: 10407990081
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Simpass Plus RX Cateter Balão para PTCA
Risk Class IV

Registration Details

10407990081

25351533197201928

02699256000164

Company Information

Dates and Status

Jan 06, 2020

06/01/2030

09/18/2025 19:00:01

Simpass Plus RX Cateter Balão para PTCA
Risk Class IV

Registration Details

10407990081

25351533197201928

02699256000164

Company Information

Turkey
PT: TURQUIA

Dates and Status

Jan 06, 2020

06/01/2030

09/18/2025 19:00:01