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URINARY STENT - ANVISA Registration 80076809042

Access comprehensive regulatory information for URINARY STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80076809042 and manufactured by BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED. The registration is held by ARTMÉDICA - PRODUTOS MÉDICOS E HOSPITALARES LTDA 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 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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80076809042
Registration Details
ANVISA Registration Number: 80076809042
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Device Details

Durasil Ureteral Stent Set with Hydrophilic Guidewire
Risk Class II

Registration Details

80076809042

25351385548202445

03950712000160

Company Information

India
PT: ÍNDIA

Dates and Status

Aug 26, 2024

VIGENTE

09/18/2025 19:00:01