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"Cardele" single-use anesthesia needle - Taiwan Registration ff1d9059a5d1e31ff0dffabe353e26c6

Access comprehensive regulatory information for "Cardele" single-use anesthesia needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ff1d9059a5d1e31ff0dffabe353e26c6 and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. The authorized representative in Taiwan is ACE TW KY 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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ff1d9059a5d1e31ff0dffabe353e26c6
Registration Details
Taiwan FDA Registration: ff1d9059a5d1e31ff0dffabe353e26c6
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Device Details

"Cardele" single-use anesthesia needle
TW: โ€œๅบทๅพท่Šโ€ไธ€ๆฌกๆ€งไฝฟ็”จ้บป้†‰้‡
Risk Class 2

Registration Details

ff1d9059a5d1e31ff0dffabe353e26c6

DHA09200057600

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5150 ้บป้†‰ๅ‚ณ่ผธ็ฉฟๅˆบ้‡

Input;; Chinese goods

Dates and Status

Feb 14, 2014

Feb 14, 2029