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"Viaan" high-frequency oscillating breathing apparatus tubing (unsterilized) - Taiwan Registration 8551b1681890cc1f16c6af580086713e

Access comprehensive regulatory information for "Viaan" high-frequency oscillating breathing apparatus tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8551b1681890cc1f16c6af580086713e and manufactured by Vyaire Medical, Inc.. The authorized representative in Taiwan is TRANSCORE TAIWAN CO., LTD..

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8551b1681890cc1f16c6af580086713e
Registration Details
Taiwan FDA Registration: 8551b1681890cc1f16c6af580086713e
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Device Details

"Viaan" high-frequency oscillating breathing apparatus tubing (unsterilized)
TW: ใ€ๅ‰ไบžๅฎ‰ใ€ž้ซ˜้ ปๆŒฏ็›ชๅ‘ผๅธๅ™จ็ฎก่ทฏ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8551b1681890cc1f16c6af580086713e

DHA04400822801

Company Information

United States

Product Details

Limited to the first level identification range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5975 Respirator Tubing

import

Dates and Status

Oct 20, 2009

Oct 20, 2024