Taiwan FDA registration d5f7b5e118e4e268479eb1e8d60284f1
"Siemens" 1650 Biochemistry Analyzer (Unsterilized)
TW: "西門子"1650生化分析儀 (未滅菌)
Taiwan·Risk Class 1·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Aug 21, 2008 – Aug 21, 2018CancelledRegistration details
- Analysis ID
- d5f7b5e118e4e268479eb1e8d60284f1
- Customs Code
- DHA04400700907
Company information
- Manufacturer
- JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices. Usage Dosage =
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2008
- Expiry Date
- Aug 21, 2018
- Cancellation Date
- Apr 10, 2020
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Siemens" 1650 Biochemistry 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 d5f7b5e118e4e268479eb1e8d60284f1 and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.
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