Taiwan FDA registration 4b2695049410c037a1f95de75f4ed839
"WRP" Patient Examination Glove (Non-Sterile)
TW: "達安倍" 病患檢查用手套 (未滅菌)
Taiwan·Risk Class 1·MD·WRP ASIA PACIFIC SDN BHD·Registered Jan 17, 2018 – Jan 17, 2028ActiveRegistration details
- Analysis ID
- 4b2695049410c037a1f95de75f4ed839
- License Form
- Ministry of Health Medical Device Import No. 018734
- Customs Code
- DHA09401873402
Company information
- Manufacturer
- WRP ASIA PACIFIC SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
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)
- J6250 Gloves for patient examination
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Jan 17, 2018
- Expiry Date
- Jan 17, 2028
About this record
Access comprehensive regulatory information for "WRP" Patient Examination Glove (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4b2695049410c037a1f95de75f4ed839 and manufactured by WRP ASIA PACIFIC SDN BHD. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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