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"Pentax" Stella uses a tourniquet single-use - Taiwan Registration 7f66b1123e1cc7ee38a591d4f50b44de

Access comprehensive regulatory information for "Pentax" Stella uses a tourniquet single-use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f66b1123e1cc7ee38a591d4f50b44de and manufactured by JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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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7f66b1123e1cc7ee38a591d4f50b44de
Registration Details
Taiwan FDA Registration: 7f66b1123e1cc7ee38a591d4f50b44de
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Device Details

"Pentax" Stella uses a tourniquet single-use
TW: โ€œ่ณ“ๅพ—โ€ๆ–ฝ้ป›ๆ‹‰ไธ€ๆฌกๆ€งไฝฟ็”จๆญข่ก€ๅคพ
Risk Class 2

Registration Details

7f66b1123e1cc7ee38a591d4f50b44de

DHA09200141708

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Chinese goods;; input

Dates and Status

Oct 31, 2022

Oct 31, 2027