Taiwan FDA registration 9336ba57412c896df795dc91b86cefb0
Lumipulse G BNP Calibrators set
TW: 錄秘帕斯GB型利納尿胜校正液組
Taiwan·Risk Class 2·MD·FUJIREBIO INC., HACHIOJI FACILITY·Registered Dec 06, 2018 – Dec 06, 2028ActiveRegistration details
- Analysis ID
- 9336ba57412c896df795dc91b86cefb0
- License Form
- Ministry of Health Medical Device Import No. 031820
- Customs Code
- DHA05603182001
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 the test reagent of sodium diuretic type of Secret Paz GB.
- 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
- Dec 06, 2018
- Expiry Date
- Dec 06, 2028
About this record
Access comprehensive regulatory information for Lumipulse G BNP 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 9336ba57412c896df795dc91b86cefb0 and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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