Taiwan FDA registration 3eed44199b20567d2cf3044c1f8d4e5a

Lumipulse G B·R·A·H·M·S PCT Calibrators set

TW: 錄秘帕斯G前降鈣素校正液組

Taiwan·Risk Class 2·MD·FUJIREBIO INC., HACHIOJI FACILITY·Registered Jan 29, 2019 – Jan 29, 2029Active

Registration details

Analysis ID: 3eed44199b20567d2cf3044c1f8d4e5a
License Form: Ministry of Health Medical Device Import No. 032150
Customs Code: DHA05603215000

Company information

Manufacturer: FUJIREBIO INC., HACHIOJI FACILITY
Manufacturer Country: Japan
Authorized Representative: Grand Marquis IVD CO., LTD.

Product details

Intended Use: This product is a calibration solution for the pre-calcitonin test reagent of Secret Paz G.
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: Jan 29, 2019
Expiry Date: Jan 29, 2029

About this record

Access comprehensive regulatory information for Lumipulse G B·R·A·H·M·S PCT 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 3eed44199b20567d2cf3044c1f8d4e5a and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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