Taiwan FDA registration 36cb51b13bf41fec7cfdbd19128d77c4
"KDL" single-use rinse needle (sterilized)
TW: “康德萊”一次性使用沖洗針 (滅菌)
Taiwan·Risk Class 1·ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD·Registered Feb 21, 2012 – Feb 21, 2017CancelledRegistration details
- Analysis ID
- 36cb51b13bf41fec7cfdbd19128d77c4
- Customs Code
- DHA04600159200
Company information
- Manufacturer
- ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- KENYEN INTERNATIONAL INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; QMS/QSD;; Chinese goods
Dates and status
- Registration Date
- Feb 21, 2012
- Expiry Date
- Feb 21, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
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..
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