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Biopsy Forceps - ANVISA Registration 80286580022

Access comprehensive regulatory information for Biopsy Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80286580022 and manufactured by JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.. The registration is held by C.M.H. COMÉRCIO DE MATERIAIS 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 Jiuhong, CHANGZHOU HEALTH MICROPORT MEDICAL DEVICES 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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80286580022
Registration Details
ANVISA Registration Number: 80286580022
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Device Details

Disposable Biopsy Forceps
Risk Class I

Registration Details

80286580022

25351151251202135

07344742000183

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 02, 2021

VIGENTE

09/18/2025 19:00:01