Taiwan FDA registration 4d5d58b3f49551f015c7345bc345e8ac

"Eccleres" laryngeal flash endoscope (unsterilized)

TW: "艾克萊理斯" 喉頭閃頻內視鏡 (未滅菌)

Taiwan·Risk Class 1·EUSA GLOBAL LLC;; ECLERIS USA·Registered Sep 16, 2014 – Sep 16, 2029Active

Registration details

Analysis ID: 4d5d58b3f49551f015c7345bc345e8ac
Customs Code: DHA09401450108

Company information

Manufacturer: EUSA GLOBAL LLC;; ECLERIS USA
Manufacturer Country: United States
Authorized Representative: BOYANG MEDICAL TECHNOLOGY CO., LTD

Product details

Intended Use: It is limited to the first level of identification scope of the "Laryngeal Strobe Endoscopy (G.4750)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4750 Throat frequented internal mirrors
Import Information: import

Dates and status

Registration Date: Sep 16, 2014
Expiry Date: Sep 16, 2029

About this record

Access comprehensive regulatory information for "Eccleres" laryngeal flash endoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4d5d58b3f49551f015c7345bc345e8ac and manufactured by EUSA GLOBAL LLC;; ECLERIS USA. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

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