Taiwan FDA registration 55fc033e1d0277f296dc59b9496845b3
"Wenli Asia Pacific" Delmar Inspection Gloves (Powder-free) (Unsterilized)
TW: "溫利亞太" 德瑪檢驗手套 (無粉)(未滅菌)
Taiwan·Risk Class 1·WRP ASIA PACIFIC SDN BHD·Registered Aug 26, 2010 – Aug 26, 2025ExpiredRegistration details
- Analysis ID
- 55fc033e1d0277f296dc59b9496845b3
- Customs Code
- DHA04400913601
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 Classification and Grading of Medical Equipment "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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Aug 26, 2010
- Expiry Date
- Aug 26, 2025
About this record
Access comprehensive regulatory information for "Wenli Asia Pacific" Delmar 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 55fc033e1d0277f296dc59b9496845b3 and manufactured by WRP ASIA PACIFIC SDN BHD. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..
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