Taiwan FDA registration 80614f0061c91c5287dd7d478006f220
Primmus CLC385 Automatic High Pressure Liquid Chromatography Instrument
TW: 普林莫斯CLC385全自動高壓液相層析儀
Registration details
- Analysis ID
- 80614f0061c91c5287dd7d478006f220
- Customs Code
- DHA04400255101
Company information
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- An analyzer for the automatic quantitative detection of glycosylated hemoglobin and mutated hemoglobin by high-pressure liquid chromatography.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2260 High-pressure liquid chromatography for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Jan 23, 2006
- Expiry Date
- Jan 23, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Primmus CLC385 Automatic High Pressure Liquid Chromatography Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80614f0061c91c5287dd7d478006f220 and manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech). The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
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