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"Phonak" Air conduction Hearing Aid (Non-Sterile) - Taiwan Registration 7c6a942a2c415f508c2f0f18814a0a4e

Access comprehensive regulatory information for "Phonak" Air conduction Hearing Aid (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7c6a942a2c415f508c2f0f18814a0a4e and manufactured by PHONAK AG. The authorized representative in Taiwan is Miaoyin Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including PHONAK OPERATION CENTER VIETNAM CO. LTD., Sonova Operation Center Vietnam Co., Ltd, and 3 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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7c6a942a2c415f508c2f0f18814a0a4e
Registration Details
Taiwan FDA Registration: 7c6a942a2c415f508c2f0f18814a0a4e
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Device Details

"Phonak" Air conduction Hearing Aid (Non-Sterile)
TW: "ๅณฏๅŠ›" ๆฐฃๅฐŽๅผๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

7c6a942a2c415f508c2f0f18814a0a4e

Ministry of Health Medical Device Import No. 016950

DHA09401695008

Company Information

Switzerland

Product Details

G ENT device

G3300 hearing aid

Imported from abroad

Dates and Status

Sep 01, 2016

Sep 01, 2021

Mar 19, 2020

Cancellation Information

Logged out

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