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"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.

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36cb51b13bf41fec7cfdbd19128d77c4
Registration Details
Taiwan FDA Registration: 36cb51b13bf41fec7cfdbd19128d77c4
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Device Details

"KDL" single-use rinse needle (sterilized)
TW: โ€œๅบทๅพท่Šโ€ไธ€ๆฌกๆ€งไฝฟ็”จๆฒ–ๆด—้‡ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

36cb51b13bf41fec7cfdbd19128d77c4

DHA04600159200

Company Information

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

Logged out

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