Taiwan FDA registration ee19ca1c376d8138e8a6a29518774d93
Medifang artificial skin OK (sterilization)
TW: 美迪芳 人工皮OK絆(滅菌)
Taiwan·Risk Class 1·Genewel Co., Ltd.·Registered May 29, 2023 – May 29, 2028ActiveRegistration details
- Analysis ID
- ee19ca1c376d8138e8a6a29518774d93
- Customs Code
- DHA09402313803
Company information
- Manufacturer
- Genewel Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CHI FU TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma covering materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- May 29, 2023
- Expiry Date
- May 29, 2028
About this record
Access comprehensive regulatory information for Medifang artificial skin OK (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ee19ca1c376d8138e8a6a29518774d93 and manufactured by Genewel Co., Ltd.. The authorized representative in Taiwan is CHI FU TRADING CO., LTD..
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