Taiwan FDA registration f741287e5e33f510a706111e8b7b2096

"Teleflex" evokes spirometer

TW: “泰利福” 誘發性肺量計

Taiwan·Risk Class 2·Teleflex Medical; Teleflex Medical de México, S. de R.L. de C.V.·Registered Jul 10, 2022 – Jul 10, 2027Active

Registration details

Analysis ID: f741287e5e33f510a706111e8b7b2096
Customs Code: DHA05603552700

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: Jul 10, 2022
Expiry Date: Jul 10, 2027

About this record

Access comprehensive regulatory information for "Teleflex" evokes spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f741287e5e33f510a706111e8b7b2096 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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