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"Vibim" tubing fixture (unsterilized) - Taiwan Registration ae60500240a47e3401009338df2879a5

Access comprehensive regulatory information for "Vibim" tubing fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae60500240a47e3401009338df2879a5 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..

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ae60500240a47e3401009338df2879a5
Registration Details
Taiwan FDA Registration: ae60500240a47e3401009338df2879a5
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Device Details

"Vibim" tubing fixture (unsterilized)
TW: "็ถญๆฏ”ๅง†" ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ae60500240a47e3401009338df2879a5

DHA04401138600

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".

D Anesthesiology

D.5770 ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ

import

Dates and Status

Feb 17, 2012

Feb 17, 2017

Dec 13, 2019

Cancellation Information

Logged out

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