Taiwan FDA registration 257f6db93fabf42a1bd4dfd163684b9a

"Telifes" manual instruments for general surgery (unsterilized)　

TW: “泰利芙斯”一般手術用手動式器械 (未滅菌)　

Taiwan·Risk Class 1·Teleflex Medical·Registered Apr 07, 2011 – Apr 07, 2026Expired

Registration details

Analysis ID: 257f6db93fabf42a1bd4dfd163684b9a
Customs Code: DHA04401015107

Company information

Manufacturer: Teleflex Medical
Manufacturer Country: United States
Authorized Representative: ASIA EAGLE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Apr 07, 2011
Expiry Date: Apr 07, 2026

About this record

Access comprehensive regulatory information for "Telifes" manual instruments for general surgery (unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 257f6db93fabf42a1bd4dfd163684b9a and manufactured by Teleflex Medical. The authorized representative in Taiwan is ASIA EAGLE CO., LTD..

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