Taiwan FDA registration a1823ab72116bc44241d7e9d40d5f9e4

BD Onclarity HPV Assay Reagent Pack

TW: BD 人類乳突病毒分型檢驗試劑

Taiwan·Risk Class 3·MD·BECTON, DICKINSON AND COMPANY·Registered May 29, 2019 – May 29, 2024Expired

Registration details

Analysis ID: a1823ab72116bc44241d7e9d40d5f9e4
License Form: Ministry of Health Medical Device Import No. 032441
Customs Code: DHA05603244101

Company information

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

Product details

Intended Use: For details, please refer to the approved version of the Chinese manual
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C0004 Human papillomavirus serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: May 29, 2019
Expiry Date: May 29, 2024

About this record

Access comprehensive regulatory information for BD Onclarity HPV Assay Reagent Pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a1823ab72116bc44241d7e9d40d5f9e4 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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