Taiwan FDA registration e04bb092cca8f532cb3c941f29f7ca37

"Leica" Bond Ready-to-Use Primary Antibody Thyroid Stimulating Hormone (QB2/6) (Non-Sterile)

TW: “錸卡”邦德即用型促甲狀腺激素一級抗體(QB2/6) (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·LEICA BIOSYSTEMS NEWCASTLE LTD.·Registered Dec 05, 2018 – Dec 05, 2028Active
Registration details
Analysis ID
e04bb092cca8f532cb3c941f29f7ca37
License Form
Ministry of Health Medical Device Import No. 019888
Customs Code
DHA09401988805
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
Dec 05, 2018
Expiry Date
Dec 05, 2028
About this record

Access comprehensive regulatory information for "Leica" Bond Ready-to-Use Primary Antibody Thyroid Stimulating Hormone (QB2/6) (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 e04bb092cca8f532cb3c941f29f7ca37 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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