Taiwan FDA registration 8551b1681890cc1f16c6af580086713e

"Viaan" high-frequency oscillating breathing apparatus tubing (unsterilized)

TW: 〝偉亞安〞高頻振盪呼吸器管路(未滅菌)

Taiwan·Risk Class 1·Vyaire Medical, Inc.·Registered Oct 20, 2009 – Oct 20, 2024Expired

Registration details

Analysis ID: 8551b1681890cc1f16c6af580086713e
Customs Code: DHA04400822801

Company information

Manufacturer: Vyaire Medical, Inc.
Manufacturer Country: United States
Authorized Representative: TRANSCORE TAIWAN CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5975 Respirator Tubing
Import Information: import

Dates and status

Registration Date: Oct 20, 2009
Expiry Date: Oct 20, 2024

About this record

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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