"KDL" single-use rinse needle (sterilized) - Taiwan Registration 36cb51b13bf41fec7cfdbd19128d77c4
Access comprehensive regulatory information for "KDL" single-use rinse needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 36cb51b13bf41fec7cfdbd19128d77c4 and manufactured by ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is KENYEN INTERNATIONAL INC..
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.
Device Details
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
I General, Plastic Surgery and Dermatology
I.4800 Hand Instruments for General Surgery
Input;; QMS/QSD;; Chinese goods
Dates and Status
Feb 21, 2012
Feb 21, 2017
Nov 04, 2019
Cancellation Information
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