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"Fu Sheng" single-use electronic bladder renal pelvis endoscope - Taiwan Registration 319c8ed4919c77087be7e0248c49dc5e

Access comprehensive regulatory information for "Fu Sheng" single-use electronic bladder renal pelvis endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 319c8ed4919c77087be7e0248c49dc5e and manufactured by ZHUHAI PUSEN MEDICAL TECHNOLOGY CO., LTD. The authorized representative in Taiwan is CANASONIC 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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319c8ed4919c77087be7e0248c49dc5e
Registration Details
Taiwan FDA Registration: 319c8ed4919c77087be7e0248c49dc5e
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Device Details

"Fu Sheng" single-use electronic bladder renal pelvis endoscope
TW: โ€œ็”ซ็ฌ™โ€ไธ€ๆฌกๆ€งไฝฟ็”จ้›ปๅญ่†€่ƒฑ่…Ž็›‚ๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

319c8ed4919c77087be7e0248c49dc5e

DHA09200148308

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

Jul 19, 2023

Jul 19, 2028