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

URINARY STENT - ANVISA Registration 80073110104

Access comprehensive regulatory information for URINARY STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80073110104 and manufactured by UROTECH GmbH. The registration is held by MEDI-GLOBE BRASIL LTDA with validity until Apr 01, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, BOSTON SCIENTIFIC 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
80073110104
2 Related Devices
Registration Details
ANVISA Registration Number: 80073110104
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

CATETER PARA PIELOPLASTIA
Risk Class III

Registration Details

80073110104

25351220058201712

04242860000192

Company Information

UROTECH GmbH
Germany
PT: ALEMANHA

Dates and Status

Apr 01, 2019

01/04/2029

09/18/2025 19:00:01

CATETER PARA PIELOPLASTIA
Risk Class III

Registration Details

80073110104

25351220058201712

04242860000192

Company Information

Dates and Status

Apr 01, 2019

01/04/2029

09/18/2025 19:00:01