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"Meidus" cardiopulmonary vascular bypass aid device (unsterilized) - Taiwan Registration ce9cbe49f2d4924736b7f26de882b20b

Access comprehensive regulatory information for "Meidus" 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 ce9cbe49f2d4924736b7f26de882b20b and manufactured by MEDOS MEDIZINTECHNIK AG. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..

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ce9cbe49f2d4924736b7f26de882b20b
Registration Details
Taiwan FDA Registration: ce9cbe49f2d4924736b7f26de882b20b
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Device Details

"Meidus" cardiopulmonary vascular bypass aid device (unsterilized)
TW: "็พŽๅพทๆ€" ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ce9cbe49f2d4924736b7f26de882b20b

DHA04401295900

Company Information

Germany

Product Details

Limited to the first level recognition range of medical equipment management measures cardiopulmonary vascular bypass auxiliary equipment (E.4200).

E Cardiovascular Medicine Science

E.4200 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™

import

Dates and Status

May 01, 2013

May 01, 2023