Taiwan FDA registration 90593294733c4812d1a68e7caf5e12f9

"Termao" Kapils membrane artificial lung

TW: "泰爾茂" 喀皮爾斯膜式人工肺

Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Oct 08, 2004 – Oct 08, 2019Cancelled

Registration details

Analysis ID: 90593294733c4812d1a68e7caf5e12f9
Customs Code: DHA00601087605

Company information

Manufacturer: TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION
Manufacturer Country: Japan
Authorized Representative: TERUMO TAIWAN MEDICAL CO., LTD.

Product details

Intended Use: It is suitable for heart-lung vascular bypass for up to six hours during open-heart surgery. The hard-shell tank is also suitable for vacuum venous drainage, where autologous blood is returned to the patient during postoperative thoracic drainage and autologous transfusion procedures.
Product Type (Level 1): E Cardiovascular Medicine Science
Import Information: import

Dates and status

Registration Date: Oct 08, 2004
Expiry Date: Oct 08, 2019
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Termao" Kapils membrane artificial lung in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90593294733c4812d1a68e7caf5e12f9 and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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