Taiwan FDA registration 0a7f609289f75b8366c97e48fda4fbbe
“KDL” SCALP VEIN SET
TW: “康德萊”頭皮針
Taiwan·Risk Class 2·MD·Zhejiang Kindly Medical Devices Co., Ltd.·Registered Mar 19, 2014 – Mar 19, 2024ExpiredRegistration details
- Analysis ID
- 0a7f609289f75b8366c97e48fda4fbbe
- License Form
- Ministry of Health Medical Device Land Transport No. 000585
- Customs Code
- DHA09200058501
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)
- J5440 Intravascular infusion sleeve
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Mar 19, 2014
- Expiry Date
- Mar 19, 2024
About this record
Access comprehensive regulatory information for “KDL” SCALP VEIN SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a7f609289f75b8366c97e48fda4fbbe and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. The authorized representative in Taiwan is KENYEN INTERNATIONAL INC..
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