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MED-EL Audio Processor - Taiwan Registration 6972e41cd978b5b5a03ab9cd5f692530

Access comprehensive regulatory information for MED-EL Audio Processor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6972e41cd978b5b5a03ab9cd5f692530 and manufactured by MED-EL Elektromedizinische Gerรคte GmbH. The authorized representative in Taiwan is MELODY MEDICAL INSTRUMENTS CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MED-EL Elektromedizinische Gerรคte GmbH, and 4 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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6972e41cd978b5b5a03ab9cd5f692530
Registration Details
Taiwan FDA Registration: 6972e41cd978b5b5a03ab9cd5f692530
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Device Details

MED-EL Audio Processor
TW: ็พŽๆจ‚่ฟช่ฒ้Ÿณ่™•็†ๅ™จ
Risk Class 3
MD

Registration Details

6972e41cd978b5b5a03ab9cd5f692530

Ministry of Health Medical Device Import No. 034137

DHA05603413705

Company Information

Product Details

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

G ENT device

G0001 Cochlear implant

Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"

Dates and Status

Dec 30, 2020

Dec 30, 2025

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