Taiwan FDA registration 005b29360869a1806d595cd3b1835960

"Leica" Novocastra Liquid Rabbit Monoclonal Antibody c-kit Oncoprotein (CD117) (Non-Sterile)

TW: "錸卡" 諾摩凱斯特兔子抗 c-kit 致癌蛋白單株抗體 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·LEICA BIOSYSTEMS NEWCASTLE LTD.·Registered Jul 20, 2018 – Jul 20, 2028Active
Registration details
Analysis ID
005b29360869a1806d595cd3b1835960
License Form
Ministry of Health Medical Device Import No. 019336
Customs Code
DHA09401933605
Company information
Manufacturer Country
United Kingdom
Product details
Intended Use
Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B1860 Immunopathological histochemical reagents and kits
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 20, 2018
Expiry Date
Jul 20, 2028
About this record

Access comprehensive regulatory information for "Leica" Novocastra Liquid Rabbit Monoclonal Antibody c-kit Oncoprotein (CD117) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 005b29360869a1806d595cd3b1835960 and manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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