Taiwan FDA registration 0b7dc8c59d22b318dc67a0efa43e29dd
"Siemens" automatic urinalysis system flushing solution
TW: "西門子" 自動尿液分析系統沖洗液
Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered May 04, 2010 – May 04, 2015CancelledRegistration details
- Analysis ID
- 0b7dc8c59d22b318dc67a0efa43e29dd
- Customs Code
- DHA04400879609
Company information
- Manufacturer Country
- United States
- 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
- May 04, 2010
- Expiry Date
- May 04, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Siemens" automatic urinalysis system flushing solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b7dc8c59d22b318dc67a0efa43e29dd and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS LIMITED.
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