Taiwan FDA registration 3e3880320cacbf2bb82879c90f231b41

"Bidi" plasma pneumoniae deoxyribonucleic acid identification reagent

TW: "必帝" 肺炎漿原體去氧核糖核酸鑑定試劑

Taiwan·Risk Class 1·BECTON, DICKINSON AND COMPANY (BD)·Registered Mar 30, 2006 – Mar 30, 2011Cancelled

Registration details

Analysis ID: 3e3880320cacbf2bb82879c90f231b41
Customs Code: DHA04400332408

Company information

Manufacturer: BECTON, DICKINSON AND COMPANY (BD)
Manufacturer Country: United States
Authorized Representative: Taiwan Branch of American Business Bidi Co., Ltd

Product details

Intended Use: BD ProbeTec ET去氧核糖核酸物質放大分析,必須與BD ProbeTec ET System搭配使用,利用Strand Displacement Amplification 〈SDA〉之技術分析可用於具臨床症狀及其他診斷證明感染肺炎的病人.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3300 嗜血桿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Mar 30, 2006
Expiry Date: Mar 30, 2011
Cancellation Date: Oct 26, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Bidi" plasma pneumoniae deoxyribonucleic acid identification reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e3880320cacbf2bb82879c90f231b41 and manufactured by BECTON, DICKINSON AND COMPANY (BD). The authorized representative in Taiwan is Taiwan Branch of American Business Bidi Co., Ltd.

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