Taiwan FDA registration aed3216d33e7742347a80083f5e41925

"Esther portable clinical analyzer"

TW: "艾斯特" 攜帶式臨床分析儀

Taiwan·Risk Class 2·ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD·Registered Nov 27, 2005 – Nov 27, 2020Cancelled

Registration details

Analysis ID: aed3216d33e7742347a80083f5e41925
Customs Code: DHA00601503102

Company information

Manufacturer: ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD
Manufacturer Country: United States;;Singapore
Authorized Representative: EVERMEDICAL COMPANY LTD.

Product details

Intended Use: Measurement of gases, electrolytes, chemicals, clotting factors, cardiac markers in the blood.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1120 血內氣體(PCO2,PO2)及血液pH值試驗系統
Import Information: import

Dates and status

Registration Date: Nov 27, 2005
Expiry Date: Nov 27, 2020
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Esther portable clinical analyzer" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aed3216d33e7742347a80083f5e41925 and manufactured by ABBOTT POINT OF CARE INC.;; FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD. The authorized representative in Taiwan is EVERMEDICAL COMPANY LTD..

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