Taiwan FDA registration a5dfc4e28a4dfda96de95998900787fe
"Molnlycke" Mepitel One Soft Silicone Wound Contact Layer (Sterile)
TW: "美尼克"美皮通單邊矽膠敷料(滅菌)
Registration details
- Analysis ID
- a5dfc4e28a4dfda96de95998900787fe
- License Form
- Department of Health Medical Device Import No. 010332
- Customs Code
- DHA04401033201
Company information
- Manufacturer Country
- Sweden;;Finland
- Authorized Representative
- ALSTRONG SCIENTIFIC INTERNATIONAL LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4018 Hydrophilic trauma coverings
- Import Information
- Imported from abroad; Contract manufacturing
Dates and status
- Registration Date
- May 10, 2011
- Expiry Date
- May 10, 2026
About this record
Access comprehensive regulatory information for "Molnlycke" Mepitel One Soft Silicone Wound Contact Layer (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5dfc4e28a4dfda96de95998900787fe and manufactured by MOLNLYCKE HEALTH CARE OY;;MOLNLYCKE HEALTH CARE AB. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL 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