URINARY STENT - ANVISA Registration 10430310200

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 10430310200 and manufactured by COLOPLAST A/S. The registration is held by COLOPLAST DO BRASIL LTDA. with validity until Sep 05, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.

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10430310200
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Registration Details
ANVISA Registration Number: 10430310200
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

BIOSOFT DUO – CATETER URETERAL DUPLO JOTA
Risk Class III

Registration Details

10430310200

25351311646202101

02794555000340

Company Information

COLOPLAST A/S
Denmark
PT: DINAMARCA

Dates and Status

Sep 05, 2022

05/09/2032

09/18/2025 19:00:01

BIOSOFT DUO – CATETER URETERAL DUPLO JOTA
Risk Class III

Registration Details

10430310200

25351311646202101

02794555000340

Company Information

Dates and Status

Sep 05, 2022

05/09/2032

09/18/2025 19:00:01