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Taiwan FDA registration 0e34d078fa47d4ac1a4a0f86f92609e6

Sismer Direct Bilirubin Reagent A

TW: 西斯美直接膽紅素試劑A
Taiwan flagTaiwan·Risk Class 2·SYSMEX INTERNATIONAL REAGENTS CO., LTD. SEISHIN FACTORY·Registered Aug 30, 2005 – Aug 30, 2015Cancelled
Registration details
Analysis ID
0e34d078fa47d4ac1a4a0f86f92609e6
Customs Code
DHA00601215008
Company information
Manufacturer
SYSMEX INTERNATIONAL REAGENTS CO., LTD. SEISHIN FACTORY
Manufacturer Country
Japan
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
It is used for the determination of direct bilirubin in serum or plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Import Information
import
Dates and status
Registration Date
Aug 30, 2005
Expiry Date
Aug 30, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for Sismer Direct Bilirubin Reagent A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e34d078fa47d4ac1a4a0f86f92609e6 and manufactured by SYSMEX INTERNATIONAL REAGENTS CO., LTD. SEISHIN FACTORY. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

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