Taiwan FDA registration bd4805ee84237d1e14682655b8045fbf

Bidi tuberculosis flora identification reagent (unsterilized)

TW: 必帝結核菌群鑑定試劑(未滅菌)

Taiwan·Risk Class 1·BECTON, DICKINSON AND COMPANY (BD)·Registered Aug 05, 2009 – Aug 05, 2019Cancelled

Registration details

Analysis ID: bd4805ee84237d1e14682655b8045fbf
Customs Code: DHA04400796501

Company information

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

Product details

Intended Use: Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3370 結核桿菌免疫螢光試劑
Import Information: import

Dates and status

Registration Date: Aug 05, 2009
Expiry Date: Aug 05, 2019
Cancellation Date: Jun 07, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Bidi tuberculosis flora identification reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd4805ee84237d1e14682655b8045fbf and manufactured by BECTON, DICKINSON AND COMPANY (BD). The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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