Taiwan FDA registration 5d42d046581b12cf3a1c9b947740ff87
"Hefeng" Wound Debridement Repair Gel (Sterilized)
TW: "和豐" 傷口清創修護凝膠 (滅菌)
Taiwan·Risk Class 1·PHARMAPLAST S.A.E.·Registered Apr 13, 2016 – Apr 13, 2026ExpiredRegistration details
- Analysis ID
- 5d42d046581b12cf3a1c9b947740ff87
- Customs Code
- DHA09401638503
Company information
- Manufacturer
- PHARMAPLAST S.A.E.
- Manufacturer Country
- Egypt
- Authorized Representative
- HORIZON INSTRUMENTS 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 13, 2016
- Expiry Date
- Apr 13, 2026
About this record
Access comprehensive regulatory information for "Hefeng" Wound Debridement Repair Gel (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5d42d046581b12cf3a1c9b947740ff87 and manufactured by PHARMAPLAST S.A.E.. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..
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