Taiwan FDA registration 35fdeb5573d30e23956c5a13a58e0770

"Telifes" microsurgical instruments (unsterilized)

TW: "泰利芙斯"顯微手術器械(未滅菌)

Taiwan·Risk Class 1·Teleflex Medical·Registered Apr 08, 2011 – Apr 08, 2026Expired

Registration details

Analysis ID: 35fdeb5573d30e23956c5a13a58e0770
Customs Code: DHA04401015900

Company information

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

Product details

Intended Use: It is limited to the first level of identification scope of the "Microsurgical Instruments (K.4525)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4525 顯微手術器械
Import Information: import

Dates and status

Registration Date: Apr 08, 2011
Expiry Date: Apr 08, 2026

About this record

Access comprehensive regulatory information for "Telifes" microsurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 35fdeb5573d30e23956c5a13a58e0770 and manufactured by Teleflex Medical. The authorized representative in Taiwan is ASIA EAGLE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.