Taiwan FDA registration 5bd4b797b459436cb1b7684f891bd22b
"Guanda" Examination Glove (Unsterilized)
TW: "觀達" 檢診手套 (未滅菌)
Taiwan·Risk Class 1·KOON SENG SDN BHD·Registered Jan 19, 2016 – Jan 19, 2021CancelledRegistration details
- Analysis ID
- 5bd4b797b459436cb1b7684f891bd22b
- Customs Code
- DHA09401608902
Company information
- Manufacturer
- KOON SENG SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- GRAND KTTA CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Gloves for Patient Examination (J.6250)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6250 病患檢查用手套
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 19, 2016
- Expiry Date
- Jan 19, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Guanda" Examination Glove (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5bd4b797b459436cb1b7684f891bd22b and manufactured by KOON SENG SDN BHD. The authorized representative in Taiwan is GRAND KTTA CO., LTD..
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