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GeneJet LiquiAid Surgical Adhesive For Hernia Mesh Fixation - Taiwan Registration c2b8e30afa7a7d4a4b8668dd5cc1b535

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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c2b8e30afa7a7d4a4b8668dd5cc1b535
Registration Details
Taiwan FDA Registration: c2b8e30afa7a7d4a4b8668dd5cc1b535
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Device Details

GeneJet LiquiAid Surgical Adhesive For Hernia Mesh Fixation
TW: ่ท็พŽๆ•ท็–ๆฐฃไฟฎ่ฃœ็ถฒ็‰‡็ต„็น”้ป่‘—ๅŠ‘
Risk Class 3
MD

Registration Details

c2b8e30afa7a7d4a4b8668dd5cc1b535

Ministry of Health Medical Device Manufacturing No. 007534

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4010 Tissue adhesives

Produced in Taiwan, China; Security monitoring

Dates and Status

Sep 16, 2022

Sep 16, 2027