Taiwan FDA registration 392d8e0fe44fd2d7326cb5dcadd65649
"Kindy" surgical covering
TW: “金蒂”外科用覆蓋巾
Taiwan·Risk Class 2·HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.·Registered Jan 08, 2016 – Jan 08, 2021CancelledRegistration details
- Analysis ID
- 392d8e0fe44fd2d7326cb5dcadd65649
- Customs Code
- DHA09200072402
Company information
- Manufacturer Country
- China
- Authorized Representative
- KING DAY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4370 Surgical drapes and accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 08, 2016
- Expiry Date
- Jan 08, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kindy" surgical covering in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 392d8e0fe44fd2d7326cb5dcadd65649 and manufactured by HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is KING DAY CO., LTD..
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