Taiwan FDA registration 1eaf3ac917e80350a7cc8774b248a006

"Adnes" Ultron artificial electronic ear

TW: “艾德尼斯”奧創人工電子耳
Taiwan flagTaiwan·Risk Class 3·ADVANCED BIONICS, LLC·Registered Sep 04, 2018 – Sep 04, 2028Active
Registration details
Analysis ID
1eaf3ac917e80350a7cc8774b248a006
Customs Code
DHA05603158800
Company information
Manufacturer Country
United States
Authorized Representative
I-LISTEN BIOTECHNOLOGICAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.0001 Artificial ear bug implanter
Import Information
Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
Registration Date
Sep 04, 2018
Expiry Date
Sep 04, 2028
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About this record

Access comprehensive regulatory information for "Adnes" Ultron artificial electronic ear in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1eaf3ac917e80350a7cc8774b248a006 and manufactured by ADVANCED BIONICS, LLC. The authorized representative in Taiwan is I-LISTEN BIOTECHNOLOGICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Advanced Bionics, LLC, and 1 recent registrations in the same category. 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.

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