Taiwan FDA registration 97b99e1721b0c32c991784d29185ef70
"Jinjiang" surgical gown
TW: “金蒂”外科用手術衣
Taiwan·Risk Class 2·HENAN KELONG MEDICAL APPARATUS AND INSTRUMENTS CO., LTD.·Registered Jan 11, 2016 – Jan 11, 2021CancelledRegistration details
- Analysis ID
- 97b99e1721b0c32c991784d29185ef70
- Customs Code
- DHA09200072501
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.4040 Clothing for medical purposes
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 11, 2016
- Expiry Date
- Jan 11, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Jinjiang" surgical gown in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97b99e1721b0c32c991784d29185ef70 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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