Taiwan FDA registration 650501aa39627858b748cab8098594b4

Hyalofast

TW: 亞羅費斯特玻尿酸軟骨修補墊
Taiwan flagTaiwan·Risk Class 3·MD·ANIKA THERAPEUTICS S.R.L.·Registered Sep 01, 2023 – Sep 01, 2028Active
Registration details
Analysis ID
650501aa39627858b748cab8098594b4
License Form
Ministry of Health Medical Device Import No. 036503
Customs Code
DHA05603650301
Company information
Manufacturer Country
Italy
Authorized Representative
YUNG JHANG CO. LTD
Product details
Intended Use
This product is a biodegradable support that captures mesenchymal stem cells to repair cartilage or osteochondral damage. It is suitable for the treatment of cartilage or osteochondral defects of knee and ankle joints.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N9999 Other
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 01, 2023
Expiry Date
Sep 01, 2028
About this record

Access comprehensive regulatory information for Hyalofast in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 650501aa39627858b748cab8098594b4 and manufactured by ANIKA THERAPEUTICS S.R.L.. The authorized representative in Taiwan is YUNG JHANG CO. LTD.

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