Taiwan FDA registration dd2c0a611dd6e7b75b72dae7562ea972
Lumipulse G PIVKA-II Calibrators set
TW: 錄秘帕斯G異常凝血酶原標準品組
Taiwan·Risk Class 2·MD·FUJIREBIO INC., HACHIOJI FACILITY·Registered Feb 20, 2014 – Feb 20, 2029ActiveRegistration details
- Analysis ID
- dd2c0a611dd6e7b75b72dae7562ea972
- License Form
- Ministry of Health Medical Device Import No. 025898
- Customs Code
- DHA05602589800
Company information
- Manufacturer
- FUJIREBIO INC., HACHIOJI FACILITY
- Manufacturer Country
- Japan
- Authorized Representative
- Grand Marquis IVD CO., LTD.
Product details
- Intended Use
- This product is used for the correction of prothrombin detection reagents for Pas G abnormalities.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 20, 2014
- Expiry Date
- Feb 20, 2029
About this record
Access comprehensive regulatory information for Lumipulse G PIVKA-II Calibrators set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd2c0a611dd6e7b75b72dae7562ea972 and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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