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"BD" Sedi-15 ESR Instrument (Non-Sterile) - Taiwan Registration 27314d04dec4822c4a344b83ff12e0c0

Access comprehensive regulatory information for "BD" Sedi-15 ESR Instrument (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 27314d04dec4822c4a344b83ff12e0c0 and manufactured by BECTON, DICKINSON AND COMPANY. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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27314d04dec4822c4a344b83ff12e0c0
Registration Details
Taiwan FDA Registration: 27314d04dec4822c4a344b83ff12e0c0
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Device Details

"BD" Sedi-15 ESR Instrument (Non-Sterile)
TW: "ๅฟ…ๅธ" ็ด…่ก€็ƒๆฒ‰ๆพฑ้€Ÿ็އๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

27314d04dec4822c4a344b83ff12e0c0

Ministry of Health Medical Device Import No. 016152

DHA09401615206

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".

B Hematology and pathology devices

B5800 Automatic Settling Rate Device

Imported from abroad

Dates and Status

Feb 04, 2016

Feb 04, 2021