Taiwan FDA registration 31e9d654661aa7066a96e8c05209f4f3

"Teleflex" evoked spirometer

TW: “泰利福” 誘發型肺量計

Taiwan·Risk Class 2·Teleflex Medical; Teleflex Medical de México, S. de R.L. de C.V.·Registered May 12, 2022 – May 12, 2027Active

Registration details

Analysis ID: 31e9d654661aa7066a96e8c05209f4f3
Customs Code: DHA05603543008

Company information

Manufacturer: Teleflex Medical; Teleflex Medical de México, S. de R.L. de C.V.
Manufacturer Country: Mexico;;United States
Authorized Representative: K&C MEDICAL CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5690 誘發型肺量計
Import Information: import

Dates and status

Registration Date: May 12, 2022
Expiry Date: May 12, 2027

About this record

Access comprehensive regulatory information for "Teleflex" evoked spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 31e9d654661aa7066a96e8c05209f4f3 and manufactured by Teleflex Medical; Teleflex Medical de México, S. de R.L. de C.V.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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