Taiwan FDA registration 86725b18bd6b884de108db278e7eb6cc

"Telifes" ENT Fiber Optic Light Source and Vehicle (Unsterilized)　

TW: "泰利芙斯" 耳鼻喉光纖光源及載具 (未滅菌)　

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

Registration details

Analysis ID: 86725b18bd6b884de108db278e7eb6cc
Customs Code: DHA04401014907

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 "ENT Fiber Optic Light Source and Vehicle (G.4350)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4350 Ear, nose and throat optical fiber light sources and carriers
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" ENT Fiber Optic Light Source and Vehicle (Unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 86725b18bd6b884de108db278e7eb6cc 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.