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"Eccleris" ENT fiber optic light source and vehicle (unsterilized) - Taiwan Registration 9e0d95d1958a891c975b2b8713951c0f

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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9e0d95d1958a891c975b2b8713951c0f
Registration Details
Taiwan FDA Registration: 9e0d95d1958a891c975b2b8713951c0f
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Device Details

"Eccleris" ENT fiber optic light source and vehicle (unsterilized)
TW: "่‰พๅ…‹่Š้‡Œๆ–ฏ" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9e0d95d1958a891c975b2b8713951c0f

DHA09401456202

Company Information

United States

Product Details

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.

G ENT Science

G.4350 Ear, nose and throat optical fiber light sources and carriers

import

Dates and Status

Oct 13, 2014

Oct 13, 2029