Taiwan FDA registration 9e0d95d1958a891c975b2b8713951c0f

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

TW: "艾克萊里斯" 耳鼻喉光纖光源及載具(未滅菌)

Taiwan·Risk Class 1·EUSA GLOBAL LLC;; ECLERIS USA·Registered Oct 13, 2014 – Oct 13, 2029Active

Registration details

Analysis ID: 9e0d95d1958a891c975b2b8713951c0f
Customs Code: DHA09401456202

Company information

Manufacturer: EUSA GLOBAL LLC;; ECLERIS USA
Manufacturer Country: United States
Authorized Representative: BOYANG MEDICAL TECHNOLOGY 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: Oct 13, 2014
Expiry Date: Oct 13, 2029

About this record

Access comprehensive regulatory information for "Eccleris" 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 9e0d95d1958a891c975b2b8713951c0f and manufactured by EUSA GLOBAL LLC;; ECLERIS USA. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

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