Taiwan FDA registration cd96dbfcd87f3ee3d9e2b67d4b514c58

"Rivanova" cardiopulmonary vascular bypass aid device (unsterilized)

TW: "里凡諾瓦"心肺血管繞道術輔助設備 (未滅菌)

Taiwan·Risk Class 1·LivaNova Deutschland GmbH·Registered Jun 21, 2010 – Jun 21, 2025Expired

Registration details

Analysis ID: cd96dbfcd87f3ee3d9e2b67d4b514c58
Customs Code: DHA04400893000

Company information

Manufacturer: LivaNova Deutschland GmbH
Manufacturer Country: Germany
Authorized Representative: INTERLINK MEDICAL ENTERPRISE CO., LTD.

Product details

Intended Use: It is limited to the first level identification scope of cardiopulmonary vascular bypass auxiliary equipment (E.4200) of the classification and grading management measures for medical devices.
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.4200 心肺血管繞道術輔助設備
Import Information: import

Dates and status

Registration Date: Jun 21, 2010
Expiry Date: Jun 21, 2025

About this record

Access comprehensive regulatory information for "Rivanova" cardiopulmonary vascular bypass aid device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd96dbfcd87f3ee3d9e2b67d4b514c58 and manufactured by LivaNova Deutschland GmbH. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..

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