Taiwan FDA registration 3ab9fc177f4601ba254a70bac52c4a8c

"Ednes" artificial electronic ear

TW: “艾德尼斯”人工電子耳
Taiwan flagTaiwan·Risk Class 3·ADVANCED BIONICS, LLC;; Advanced Bionics AG·Registered Jan 09, 2014 – Jan 09, 2024Expired
Registration details
Analysis ID
3ab9fc177f4601ba254a70bac52c4a8c
Customs Code
DHA05602575504
Company information
Manufacturer Country
United States;;Switzerland
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". Contract manufacturing
Dates and status
Registration Date
Jan 09, 2014
Expiry Date
Jan 09, 2024
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About this record

Access comprehensive regulatory information for "Ednes" 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 3ab9fc177f4601ba254a70bac52c4a8c and manufactured by ADVANCED BIONICS, LLC;; Advanced Bionics AG. The authorized representative in Taiwan is I-LISTEN BIOTECHNOLOGICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ADVANCED BIONICS, LLC;; Advanced Bionics AG, ADVANCED BIONICS LLC, and 2 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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