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"Ednes" artificial electronic ear - Taiwan Registration e259e328bdf0b03e9af4fd1f31883734

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 e259e328bdf0b03e9af4fd1f31883734 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;; Advanced Bionics AG, 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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e259e328bdf0b03e9af4fd1f31883734
Registration Details
Taiwan FDA Registration: e259e328bdf0b03e9af4fd1f31883734
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Device Details

"Ednes" artificial electronic ear
TW: โ€œ่‰พๅพทๅฐผๆ–ฏโ€ไบบๅทฅ้›ปๅญ่€ณ
Risk Class 3

Registration Details

e259e328bdf0b03e9af4fd1f31883734

DHA00602086302

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT Science

G.0001 Artificial ear bug implanter

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". input

Dates and Status

Mar 29, 2010

Mar 29, 2025

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