"Phonak" Air conduction Hearing Aid (Non-Sterile)
Taiwan·Risk Class 1·MD·PHONAK AG·Registered Sep 01, 2016 – Sep 01, 2021Cancelled- Analysis ID
- 7c6a942a2c415f508c2f0f18814a0a4e
- License Form
- Ministry of Health Medical Device Import No. 016950
- Customs Code
- DHA09401695008
- Manufacturer
- PHONAK AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- Miaoyin Medical Equipment Co., Ltd
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
- Registration Date
- Sep 01, 2016
- Expiry Date
- Sep 01, 2021
- Cancellation Date
- Mar 19, 2020
- Status
- Logged out
- Reason
- 註銷藥商許可執照
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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.