Taiwan FDA registration f6799882bf84b214a4761a79487312d2
"Cardinalai" disposable indwelling needle
TW: “康德萊”一次性使用留置針
Taiwan·Risk Class 2·ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD.·Registered Jan 24, 2013 – Jan 24, 2018CancelledRegistration details
- Analysis ID
- f6799882bf84b214a4761a79487312d2
- Customs Code
- DHA04200047804
Company information
- Manufacturer
- ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- KENYEN INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5570 Subcutaneous single-chamber needle
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 24, 2013
- Expiry Date
- Jan 24, 2018
- 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 "Cardinalai" disposable indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f6799882bf84b214a4761a79487312d2 and manufactured by ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD.. The authorized representative in Taiwan is KENYEN INTERNATIONAL INC..
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