Taiwan FDA registration 7ab5b72940f7a1ecb185860be6a268cd

BD Bardermixun disposable hollow core sectioning instrument

TW: BD 巴德密迅拋棄式空芯切片器械
Taiwan flagTaiwan·Risk Class 2·BARD PERIPHERAL VASCULAR, INC.;; CAREFUSION D.R. 203, LTD.·Registered Dec 13, 2019 – Dec 13, 2029Active
Registration details
Analysis ID
7ab5b72940f7a1ecb185860be6a268cd
Customs Code
DHA05603302209
Company information
Manufacturer Country
Dominican Republic;;United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1075 腸胃科-泌尿科生檢器械
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Dec 13, 2019
Expiry Date
Dec 13, 2029
About this record

Access comprehensive regulatory information for BD Bardermixun disposable hollow core sectioning instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7ab5b72940f7a1ecb185860be6a268cd and manufactured by BARD PERIPHERAL VASCULAR, INC.;; CAREFUSION D.R. 203, LTD.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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