Taiwan FDA registration 972c0b3c951f5694e10a4acba12c406c
“KDL” Disposable Needles
TW: “康德萊”一次性使用無菌注射針
Taiwan·Risk Class 2·MD·Zhejiang Kindly Medical Devices Co., Ltd.·Registered Aug 29, 2018 – Aug 29, 2028ActiveRegistration details
- Analysis ID
- 972c0b3c951f5694e10a4acba12c406c
- License Form
- Ministry of Health Medical Device Land Transport No. 000921
- Customs Code
- DHA09200092101
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)
- J5570 Subcutaneous single-lumen needle
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Aug 29, 2018
- Expiry Date
- Aug 29, 2028
About this record
Access comprehensive regulatory information for “KDL” Disposable Needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 972c0b3c951f5694e10a4acba12c406c and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. The authorized representative in Taiwan is KENYEN INTERNATIONAL INC..
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