Polypectomy Snare - ANVISA Registration 10259750034

Access comprehensive regulatory information for Polypectomy Snare in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10259750034 and manufactured by manufacturer not specified. The registration is held by STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE LTDA. with validity until Dec 12, 2026.

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 JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD., United States Endoscopy Group, Inc. (US Endoscopy), 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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10259750034
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Registration Details
ANVISA Registration Number: 10259750034
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Dispositivo combinado com alça e injetor iSnare
Risk Class III

Registration Details

10259750034

25351073357202018

59233783000104

Dates and Status

Mar 23, 2020

12/12/2026

09/18/2025 19:00:01

Dispositivo combinado com alça e injetor iSnare
Risk Class III

Registration Details

10259750034

25351073357202018

59233783000104

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 23, 2020

12/12/2026

09/18/2025 19:00:01