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“FUJIFILM medwork” Polypectomy Snare POL-Series - Taiwan Registration 2209ce19ecbcd8fecfb9e7d34fb4ee74

Access comprehensive regulatory information for “FUJIFILM medwork” Polypectomy Snare POL-Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2209ce19ecbcd8fecfb9e7d34fb4ee74 and manufactured by FUJIFILM medwork GmbH. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2209ce19ecbcd8fecfb9e7d34fb4ee74
Registration Details
Taiwan FDA Registration: 2209ce19ecbcd8fecfb9e7d34fb4ee74
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Device Details

“FUJIFILM medwork” Polypectomy Snare POL-Series
TW: "富士 美德沃"瘜肉切除環
Risk Class 2
MD

Registration Details

2209ce19ecbcd8fecfb9e7d34fb4ee74

Ministry of Health Medical Device Import No. 036462

DHA05603646200

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H4300 Electrosurgical device for endoscopes and accessories

Imported from abroad

Dates and Status

Apr 11, 2023

Apr 11, 2028