Taiwan FDA registration 345eb7c17762f1cde2cba0af0d5a8cbe
"Wenli Asia Pacific" Kangfu Inspection Gloves (Powder-free) (Unsterilized)
TW: "溫利亞太" 康福檢驗手套(無粉)(未滅菌)
Taiwan·Risk Class 1·WRP ASIA PACIFIC SDN BHD·Registered Aug 26, 2010 – Aug 26, 2020CancelledRegistration details
- Analysis ID
- 345eb7c17762f1cde2cba0af0d5a8cbe
- Customs Code
- DHA04400913700
Company information
- Manufacturer
- WRP ASIA PACIFIC SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- SANSOME TRADING 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
- Aug 26, 2010
- Expiry Date
- Aug 26, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Wenli Asia Pacific" Kangfu Inspection Gloves (Powder-free) (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 345eb7c17762f1cde2cba0af0d5a8cbe and manufactured by WRP ASIA PACIFIC SDN BHD. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..
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