Taiwan FDA registration ae50a411ffc1685c362dfa9be19a7cdc

"Maqida" ENT fiber optic light source and vehicle (unsterilized)

TW: "瑪戚達" 耳鼻喉光纖光源及載具 (未滅菌)

Taiwan·Risk Class 1·MACHIDA ENDOSCOPE CO. LTD.·Registered Aug 15, 2011 – Aug 15, 2026Active

Registration details

Analysis ID: ae50a411ffc1685c362dfa9be19a7cdc
Customs Code: DHA04401070307

Company information

Manufacturer: MACHIDA ENDOSCOPE CO. LTD.
Manufacturer Country: Japan
Authorized Representative: FU TAI TRADING 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 15, 2011
Expiry Date: Aug 15, 2026

About this record

Access comprehensive regulatory information for "Maqida" 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 ae50a411ffc1685c362dfa9be19a7cdc and manufactured by MACHIDA ENDOSCOPE CO. LTD.. The authorized representative in Taiwan is FU TAI TRADING 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.