Taiwan FDA registration b6ed2b34a0dbc1632d8a6c4f504ccc23

"Leica" Novocastra Liquid Mouse Monoclonal Antibody Mismatch Repair Protein 2 (MSH2) (Non-Sterile)

TW: “錸卡”諾摩凱斯特老鼠單株抗體錯誤配對修復蛋白(MSH2) (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·LEICA BIOSYSTEMS NEWCASTLE LTD.·Registered Nov 12, 2018 – Nov 12, 2028Active
Registration details
Analysis ID
b6ed2b34a0dbc1632d8a6c4f504ccc23
License Form
Ministry of Health Medical Device Import No. 019814
Customs Code
DHA09401981402
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
Nov 12, 2018
Expiry Date
Nov 12, 2028
About this record

Access comprehensive regulatory information for "Leica" Novocastra Liquid Mouse Monoclonal Antibody Mismatch Repair Protein 2 (MSH2) (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 b6ed2b34a0dbc1632d8a6c4f504ccc23 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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