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"Termao" Spistrong Putia platelet and plasma collection line - Taiwan Registration 0677468741a5155c51ed819eb47c4d5e

Access comprehensive regulatory information for "Termao" Spistrong Putia platelet and plasma collection line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0677468741a5155c51ed819eb47c4d5e and manufactured by TERUMO BCT, INC.;; TFB MANUFACTURING SRL. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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0677468741a5155c51ed819eb47c4d5e
Registration Details
Taiwan FDA Registration: 0677468741a5155c51ed819eb47c4d5e
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Device Details

"Termao" Spistrong Putia platelet and plasma collection line
TW: "ๆณฐ็ˆพ่Œ‚" ๆ€ๅ€ๅฃฏไบžๆ™ฎ็ทนไบž่ก€ๅฐๆฟๅŠ่ก€ๆผฟๆ”ถ้›†็ฎก่ทฏ
Risk Class 2

Registration Details

0677468741a5155c51ed819eb47c4d5e

DHA05603369508

Company Information

Costa Rica;;United States

Product Details

This product is used with the "Termo" Spistrong Aputia blood cell separator and can be used to collect platelets and plasma.

B Hematology, pathology, and genetics

B.9100 Containers for the collection and disposal of blood and blood components

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Oct 28, 2020

Oct 28, 2025