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"Vibim" laryngeal airway tube (unsterilized) - Taiwan Registration abfdb545d4fd48c0f6e9f54566684ae0

Access comprehensive regulatory information for "Vibim" laryngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number abfdb545d4fd48c0f6e9f54566684ae0 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..

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abfdb545d4fd48c0f6e9f54566684ae0
Registration Details
Taiwan FDA Registration: abfdb545d4fd48c0f6e9f54566684ae0
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Device Details

"Vibim" laryngeal airway tube (unsterilized)
TW: "็ถญๆฏ”ๅง†" ๅ–‰้ ญๆฐฃ้“็ฎก (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

abfdb545d4fd48c0f6e9f54566684ae0

DHA09402113500

Company Information

Germany

Product Details

Limited to the classification and grading management method of medical equipment, oropharyngeal airway canal (D.5110) first grade identification range.

D Anesthesiology

D.5110 Oropharyngeal airway tubes

Input;; QMS/QSD

Dates and Status

Dec 25, 2019

Dec 25, 2029