Polypectomy Snare - ANVISA Registration 80022060114

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 80022060114 and manufactured by FUJIFILM MEDWORK GMBH. The registration is held by FUJIFILM DO BRASIL LTDA with validity until Nov 25, 2034.

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 United States Endoscopy Group, Inc. (US Endoscopy), JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD., 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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80022060114
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Registration Details
ANVISA Registration Number: 80022060114
Janaina dos Santos de Miranda

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Related Devices (2)

Alça de Polipectomia - POL
Risk Class III

Registration Details

80022060114

25351363571202489

60397874000156

Company Information

Germany
PT: ALEMANHA

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01

Alça de Polipectomia - POL
Risk Class III

Registration Details

80022060114

25351363571202489

60397874000156

Company Information

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01