Taiwan FDA registration 931dbae787fd826b335ec0db0aedbeaa
Prinmosyot Type 2 fully automated glycoglobin analysis reagent
TW: 普林莫斯優特2型全自動化醣化血色素分析試劑
Registration details
- Analysis ID
- 931dbae787fd826b335ec0db0aedbeaa
- Customs Code
- DHA00601604801
Company information
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- The Primmos ULTRA2 fully automated glycoglobin analysis system is a high-pressure liquid chromatography method to quantify glycohemoglobin in normal or diabetic patients in vitro diagnostic tests, which can be used with whole blood or diluted samples.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7470 Analysis of glycosylated hemoglobin
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2006
- Expiry Date
- Feb 23, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Prinmosyot Type 2 fully automated glycoglobin analysis reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 931dbae787fd826b335ec0db0aedbeaa and manufactured by TRINITY BIOTECH PRIMUS CORPORATION DBA TRINITY BIOTECH. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
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