Taiwan FDA registration 980c265649db0d3774a8a8e66e2bd954
"Ngai Sheng" Patient Examination Gloves (Sterilized)
TW: "毅升" 病患檢查用手套 (滅菌)
Taiwan·Risk Class 1·Jiangsu Yaohua Medical Device Technology Co., Ltd.·Registered Mar 30, 2011 – Mar 30, 2021CancelledRegistration details
- Analysis ID
- 980c265649db0d3774a8a8e66e2bd954
- Customs Code
- DHA04600131500
Company information
- Manufacturer Country
- China
- Authorized Representative
- E-UP 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;; Input;; Chinese goods
Dates and status
- Registration Date
- Mar 30, 2011
- Expiry Date
- Mar 30, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ngai Sheng" Patient Examination Gloves (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 980c265649db0d3774a8a8e66e2bd954 and manufactured by Jiangsu Yaohua Medical Device Technology Co., Ltd.. The authorized representative in Taiwan is E-UP CO., LTD..
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