Taiwan FDA registration c2b8e30afa7a7d4a4b8668dd5cc1b535
GeneJet LiquiAid Surgical Adhesive For Hernia Mesh Fixation
TW: 荷美敷疝氣修補網片組織黏著劑
Taiwan·Risk Class 3·MD·GENEJET BIOTECH CO., LTD.·Registered Sep 16, 2022 – Sep 16, 2027ActiveRegistration details
- Analysis ID
- c2b8e30afa7a7d4a4b8668dd5cc1b535
- License Form
- Ministry of Health Medical Device Manufacturing No. 007534
Company information
- Manufacturer
- GENEJET BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENEJET BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4010 Tissue adhesives
- Import Information
- Produced in Taiwan, China; Security monitoring
Dates and status
- Registration Date
- Sep 16, 2022
- Expiry Date
- Sep 16, 2027
About this record
Access comprehensive regulatory information for GeneJet LiquiAid Surgical Adhesive For Hernia Mesh Fixation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c2b8e30afa7a7d4a4b8668dd5cc1b535 and manufactured by GENEJET BIOTECH CO., LTD.. The authorized representative in Taiwan is GENEJET BIOTECH CO., LTD..
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