Taiwan FDA registration aed572556e73be354b10c343bd318527

"Siemens" Automatic Chemical Analysis System Ion-selective Electrode Internal Reference Solution (Unsterilized)

TW: "西門子"全自動化學分析系統離子選擇性電極內部參考液 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Apr 08, 2008 – Apr 08, 2013Cancelled
Registration details
Analysis ID
aed572556e73be354b10c343bd318527
Customs Code
DHA04400664201
Company information
Manufacturer Country
United States;;Japan
Authorized Representative
SIEMENS LIMITED
Product details
Intended Use
Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.4010 Reaction Reagents for General Purposes
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Apr 08, 2008
Expiry Date
Apr 08, 2013
Cancellation Date
Aug 10, 2015
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Siemens" Automatic Chemical Analysis System Ion-selective Electrode Internal Reference Solution (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aed572556e73be354b10c343bd318527 and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

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