Taiwan FDA registration f7e44ab5a61cec7be218441661b2988c

"Tai Lifu" Manual instrument for general surgery (unsterilized)

TW: "泰利福" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·Teleflex Medical; TECOMET INC.·Registered Feb 13, 2018 – Feb 13, 2028Active

Registration details

Analysis ID: f7e44ab5a61cec7be218441661b2988c
Customs Code: DHA09401881703

Company information

Manufacturer: Teleflex Medical; TECOMET INC.
Manufacturer Country: United States
Authorized Representative: TELEFLEX MEDICAL TAIWAN 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: Feb 13, 2018
Expiry Date: Feb 13, 2028

About this record

Access comprehensive regulatory information for "Tai Lifu" Manual instrument 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 f7e44ab5a61cec7be218441661b2988c and manufactured by Teleflex Medical; TECOMET INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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