Taiwan FDA registration 607b480f4b8a5ae5f833a5c29a3a7ca9
"Menik" Lavis dressings (sterilized)
TW: “美尼克”艾薇斯 敷料 (滅菌)
Registration details
- Analysis ID
- 607b480f4b8a5ae5f833a5c29a3a7ca9
- Customs Code
- DHA04401184901
Company information
- Manufacturer
- MOLNLYCKE HEALTH CARE AB
- Manufacturer Country
- Sweden
- 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, 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
- Jun 20, 2012
- Expiry Date
- Jun 20, 2017
- Cancellation Date
- Jan 05, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Menik" Lavis 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 607b480f4b8a5ae5f833a5c29a3a7ca9 and manufactured by MOLNLYCKE HEALTH CARE AB. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..
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