Taiwan FDA registration 77b2a20022a5e47d6c2c7ea1a67853d1
“Mölnlycke” Mepilex Border Post-Op Ag
TW: “美尼克”美皮蕾防水型術後銀敷料
Taiwan·Risk Class 2·MD·Mölnlycke Health Care Oy;;Mölnlycke Health Care AB·Registered Jun 27, 2019 – Jun 27, 2024ExpiredRegistration details
- Analysis ID
- 77b2a20022a5e47d6c2c7ea1a67853d1
- License Form
- Ministry of Health Medical Device Import No. 032708
- Customs Code
- DHA05603270802
Company information
- Manufacturer Country
- Sweden;;Finland
- Authorized Representative
- ALSTRONG SCIENTIFIC INTERNATIONAL LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4018 Hydrophilic trauma coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 27, 2019
- Expiry Date
- Jun 27, 2024
About this record
Access comprehensive regulatory information for “Mölnlycke” Mepilex Border Post-Op Ag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77b2a20022a5e47d6c2c7ea1a67853d1 and manufactured by Mölnlycke Health Care Oy;;Mölnlycke Health Care AB. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..
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