Taiwan FDA registration 27314d04dec4822c4a344b83ff12e0c0

"BD" Sedi-15 ESR Instrument (Non-Sterile)

TW: "必帝" 紅血球沉澱速率儀 (未滅菌)

Taiwan·Risk Class 1·MD·BECTON, DICKINSON AND COMPANY·Registered Feb 04, 2016 – Feb 04, 2021Expired

Registration details

Analysis ID: 27314d04dec4822c4a344b83ff12e0c0
License Form: Ministry of Health Medical Device Import No. 016152
Customs Code: DHA09401615206

Company information

Manufacturer: BECTON, DICKINSON AND COMPANY
Manufacturer Country: United Kingdom
Authorized Representative: BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B5800 Automatic Settling Rate Device
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 04, 2016
Expiry Date: Feb 04, 2021

About this record

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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