Taiwan FDA registration 7f2843519d64c795811b963d8a2fac92

"Termao" artificial heart and lung new catheter sleeve

TW: “泰爾茂”人工心肺新式導管套

Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Nov 11, 2010 – Nov 11, 2025Expired

Registration details

Analysis ID: 7f2843519d64c795811b963d8a2fac92
Customs Code: DHA00602169308

Company information

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

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
Import Information: import

Dates and status

Registration Date: Nov 11, 2010
Expiry Date: Nov 11, 2025

About this record

Access comprehensive regulatory information for "Termao" artificial heart and lung new catheter sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f2843519d64c795811b963d8a2fac92 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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