Taiwan FDA registration d687b15fb9868b06f0bb64f03d84fd48
"Menick" Mepilet Waterproof Post-Surgical Elastic Silicone Dressing (Sterilization)
TW: "墨尼克"美皮蕾防水型術後彈性矽膠敷料 (滅菌)
Registration details
- Analysis ID
- d687b15fb9868b06f0bb64f03d84fd48
- Customs Code
- DHA09401418906
Company information
- Manufacturer
- MOLNLYCKE HEALTH CARE OY
- Manufacturer Country
- Finland
- Authorized Representative
- MOLNLYCKE HEALTH CARE TAIWAN 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 30, 2014
- Expiry Date
- May 30, 2029
About this record
Access comprehensive regulatory information for "Menick" Mepilet Waterproof Post-Surgical Elastic Silicone Dressing (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d687b15fb9868b06f0bb64f03d84fd48 and manufactured by MOLNLYCKE HEALTH CARE OY. The authorized representative in Taiwan is MOLNLYCKE HEALTH CARE TAIWAN CO., LTD..
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