Taiwan FDA registration 1bd6e6d721c17d6333a1bebeb58ed6c7
"Flygt" hydrophilic dressings (sterilized)
TW: “飛力” 親水性敷料(滅菌)
Taiwan·Risk Class 1·PHARMAPLAST S.A.E.·Registered May 21, 2012 – May 21, 2027ActiveRegistration details
- Analysis ID
- 1bd6e6d721c17d6333a1bebeb58ed6c7
- Customs Code
- DHA04401172700
Company information
- Manufacturer
- PHARMAPLAST S.A.E.
- Manufacturer Country
- Egypt
- Authorized Representative
- Flygt Medical Equipment 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
- May 21, 2012
- Expiry Date
- May 21, 2027
About this record
Access comprehensive regulatory information for "Flygt" hydrophilic dressings (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1bd6e6d721c17d6333a1bebeb58ed6c7 and manufactured by PHARMAPLAST S.A.E.. The authorized representative in Taiwan is Flygt Medical Equipment Co., Ltd.
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