Taiwan FDA registration cb1fd063e89ee434ad3fc2cd8ad23e4e

"Leica" Novocastra Liquid Mouse Monoclonal Antibody Mismatch Repair Protein (MLH1) (Non-Sterile)

TW: “錸卡”諾摩凱斯特老鼠單株抗體錯誤配對修復蛋白(MLH1) (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·LEICA BIOSYSTEMS NEWCASTLE LTD.·Registered Feb 13, 2019 – Feb 13, 2024Expired
Registration details
Analysis ID
cb1fd063e89ee434ad3fc2cd8ad23e4e
License Form
Ministry of Health Medical Device Import No. 020094
Customs Code
DHA09402009407
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
Feb 13, 2019
Expiry Date
Feb 13, 2024
About this record

Access comprehensive regulatory information for "Leica" Novocastra Liquid Mouse Monoclonal Antibody Mismatch Repair Protein (MLH1) (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 cb1fd063e89ee434ad3fc2cd8ad23e4e 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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