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)
Taiwan flagTaiwan·Risk Class 1·MOLNLYCKE HEALTH CARE OY·Registered May 30, 2014 – May 30, 2029Active
Registration details
Analysis ID
d687b15fb9868b06f0bb64f03d84fd48
Customs Code
DHA09401418906
Company information
Manufacturer Country
Finland
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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices