Taiwan FDA registration 045b07e6b5d94212766a2d592880d6b4
"Siemens" 120 sheath flow fluid/rinse fluid
TW: "西門子" 120鞘流液/沖洗液
Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Mar 24, 2006 – Mar 24, 2016CancelledRegistration details
- Analysis ID
- 045b07e6b5d94212766a2d592880d6b4
- Customs Code
- DHA04400318507
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- Sheath fluid (Sheath), which encloses the sample through an optical monitor, ensures analysis of individual cells. Rinse fluid is used to clean hydraulic piping and reaction cells after each sample to prevent carryover contamination and ensure the integrity of analytical results.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Mar 24, 2006
- Expiry Date
- Mar 24, 2016
- 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" 120 sheath flow fluid/rinse fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 045b07e6b5d94212766a2d592880d6b4 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS LIMITED.
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