Taiwan FDA registration 93291928e9fb5e0c3a28867595522035

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

TW: "美恩力" 光纖光源及載具 (未滅菌)

Taiwan·Risk Class 1·JINYANG MEDICAL INSTRUMENTS CO., LTD·Registered Apr 26, 2016 – Apr 26, 2026Expired

Registration details

Analysis ID: 93291928e9fb5e0c3a28867595522035
Customs Code: DHA09600270205

Company information

Manufacturer: JINYANG MEDICAL INSTRUMENTS CO., LTD
Manufacturer Country: China
Authorized Representative: MENEY 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: Input;; Chinese goods

Dates and status

Registration Date: Apr 26, 2016
Expiry Date: Apr 26, 2026

About this record

Access comprehensive regulatory information for "Meenli" 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 93291928e9fb5e0c3a28867595522035 and manufactured by JINYANG MEDICAL INSTRUMENTS CO., LTD. The authorized representative in Taiwan is MENEY CO., LTD..

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