Taiwan FDA registration ac1ec04f3dd4db3679feec170f6ad2a6

“Terumo” BMAC2 Bone Marrow Procedure Pack

TW: “泰爾茂”必麥克處理套包

Taiwan·Risk Class 2·MD·TERUMO BCT, INC.·Registered Sep 06, 2019 – Sep 06, 2024Expired

Registration details

Analysis ID: ac1ec04f3dd4db3679feec170f6ad2a6
License Form: Ministry of Health Medical Device Import No. 032496
Customs Code: DHA05603249600

Company information

Manufacturer: TERUMO BCT, INC.
Manufacturer Country: United States
Authorized Representative: TERUMO TAIWAN MEDICAL CO., LTD.

Product details

Intended Use: This product is used with the SmartPReP3 centrifuge system to isolate bone marrow cell concentrate from bone marrow in clinical examination rooms or during surgery.
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B9245 Automatic Hematology Cell Separator
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 06, 2019
Expiry Date: Sep 06, 2024

About this record

Access comprehensive regulatory information for “Terumo” BMAC2 Bone Marrow Procedure Pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac1ec04f3dd4db3679feec170f6ad2a6 and manufactured by TERUMO BCT, INC.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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