Taiwan FDA registration 716ec1921d178c3fb958f07ff5b0af08
“AMS” LiquiBand Hernia Mesh Fixation Device
TW: “艾曼斯”立可棒疝氣修補網片黏著劑
Taiwan·Risk Class 3·MD·Advanced Medical Solutions Limited·Registered Aug 18, 2017 – Aug 18, 2027ActiveRegistration details
- Analysis ID
- 716ec1921d178c3fb958f07ff5b0af08
- License Form
- Ministry of Health Medical Device Import No. 030122
- Customs Code
- DHA05603012201
Company information
- Manufacturer
- Advanced Medical Solutions Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- MEDLION BIOTECH CO., 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)
- I4010 Tissue adhesives
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 18, 2017
- Expiry Date
- Aug 18, 2027
About this record
Access comprehensive regulatory information for “AMS” LiquiBand Hernia Mesh Fixation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 716ec1921d178c3fb958f07ff5b0af08 and manufactured by Advanced Medical Solutions Limited. The authorized representative in Taiwan is MEDLION BIOTECH CO., LTD..
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