Taiwan FDA registration 3192e076faef2b1c5500e6756ff36f4d

"Aipu" fiber optic light source and vehicle (unsterilized)　

TW: “艾普”光纖光源及載具(未滅菌)　

Taiwan·Risk Class 1·APPLIED FIBEROPTICS DIVISION OF VITALCOR, INC·Registered Aug 19, 2011 – Aug 19, 2026Active

Registration details

Analysis ID: 3192e076faef2b1c5500e6756ff36f4d
Customs Code: DHA04401073102

Company information

Manufacturer: APPLIED FIBEROPTICS DIVISION OF VITALCOR, INC
Manufacturer Country: United States
Authorized Representative: CHAMP MEDICS 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: Aug 19, 2011
Expiry Date: Aug 19, 2026

About this record

Access comprehensive regulatory information for "Aipu" 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 3192e076faef2b1c5500e6756ff36f4d and manufactured by APPLIED FIBEROPTICS DIVISION OF VITALCOR, INC. The authorized representative in Taiwan is CHAMP MEDICS CO., LTD..

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