Taiwan FDA registration 797160aa2cca4eaf50ac8b0520c39aba

"Siemens" Reference Solution Kit (for Confirmation Enzyme Immunoassay Analyzer) (Unsterilized)

TW: “西門子”參考溶液試劑組 (用於確認酵素免疫分析儀)(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Sep 15, 2010 – Sep 15, 2020Cancelled
Registration details
Analysis ID
797160aa2cca4eaf50ac8b0520c39aba
Customs Code
DHA04400919603
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1660 Quality control materials (analytical and non-analytical)
Import Information
import
Dates and status
Registration Date
Sep 15, 2010
Expiry Date
Sep 15, 2020
Cancellation Date
Feb 09, 2021
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Siemens" Reference Solution Kit (for Confirmation Enzyme Immunoassay Analyzer) (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 797160aa2cca4eaf50ac8b0520c39aba and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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