Taiwan FDA registration 96190baf51413c5dfe679b93bf1aab0b

"Telifes" Non-powered Neurosurgical Instruments (Unsterilized)

TW: "泰利芙斯" 非動力式神經外科用器械 (未滅菌)

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

Registration details

Analysis ID: 96190baf51413c5dfe679b93bf1aab0b
Customs Code: DHA04401016008

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 "Non-powered Neurosurgical Devices (K.4535)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4535 非動力式神經外科用器械
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" Non-powered Neurosurgical 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 96190baf51413c5dfe679b93bf1aab0b 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.