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"Leica" Bond Ready-to-Use Primary Antibody CD138 (MI15)(Non-Sterile) - Taiwan Registration c89aefec4e483f19dc87ea1e7a936b71

Access comprehensive regulatory information for "Leica" Bond Ready-to-Use Primary Antibody CD138 (MI15)(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 c89aefec4e483f19dc87ea1e7a936b71 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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c89aefec4e483f19dc87ea1e7a936b71
Registration Details
Taiwan FDA Registration: c89aefec4e483f19dc87ea1e7a936b71
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Device Details

"Leica" Bond Ready-to-Use Primary Antibody CD138 (MI15)(Non-Sterile)
TW: โ€œ้Œธๅกโ€้‚ฆๅพทๅณ็”จๅž‹็ดฐ่ƒžๆจ™่ชŒ138ไธ€็ดšๆŠ—้ซ”(MI15)(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c89aefec4e483f19dc87ea1e7a936b71

Ministry of Health Medical Device Import No. 019852

DHA09401985200

Company Information

Product Details

Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.

B Hematology and pathology devices

B1860 Immunopathological histochemical reagents and kits

Imported from abroad

Dates and Status

Nov 26, 2018

Nov 26, 2028