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"Seexin" electronic ureteral pyeloscope - Taiwan Registration 1d2d09f631bba8a10299c9ee989e6ca1

Access comprehensive regulatory information for "Seexin" electronic ureteral pyeloscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d2d09f631bba8a10299c9ee989e6ca1 and manufactured by Zhuhai Seesheen Medical Technology Co., Ltd.. The authorized representative in Taiwan is Kang Cheng Medical Technology 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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1d2d09f631bba8a10299c9ee989e6ca1
Registration Details
Taiwan FDA Registration: 1d2d09f631bba8a10299c9ee989e6ca1
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Device Details

"Seexin" electronic ureteral pyeloscope
TW: โ€œ่ฆ–ๆ–ฐโ€้›ปๅญ่ผธๅฐฟ็ฎก่…Ž็›‚้ก
Risk Class 2

Registration Details

1d2d09f631bba8a10299c9ee989e6ca1

DHA09200142609

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Input;; Chinese goods

Dates and Status

Jan 11, 2023

Jan 11, 2028