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"Simai" resection scope - Taiwan Registration f544ae0a5c34c8460cec602e8fc4b0be

Access comprehensive regulatory information for "Simai" resection scope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f544ae0a5c34c8460cec602e8fc4b0be and manufactured by SIMAI 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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f544ae0a5c34c8460cec602e8fc4b0be
Registration Details
Taiwan FDA Registration: f544ae0a5c34c8460cec602e8fc4b0be
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Device Details

"Simai" resection scope
TW: โ€œๅธ้‚โ€ๅˆ‡้™ค้ก
Risk Class 2

Registration Details

f544ae0a5c34c8460cec602e8fc4b0be

DHA09200130102

Company Information

China

Product Details

SMNKJ

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Chinese goods;; input

Dates and Status

Dec 09, 2021

Dec 09, 2026