"Interton" Hearing Aids (Non-Sterile)
Taiwan·Risk Class 1·MD·INTERTON A/S·Registered Sep 30, 2016 – Sep 30, 2021Cancelled- Analysis ID
- b91f3aa40f16f626b408f0efc9d0b609
- License Form
- Ministry of Health Medical Device Import No. 017037
- Customs Code
- DHA09401703701
- Manufacturer
- INTERTON A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Hongyun 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 30, 2016
- Expiry Date
- Sep 30, 2021
- Cancellation Date
- Jan 18, 2019
- Status
- Logged out
- Reason
- 公司歇業
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Access comprehensive regulatory information for "Interton" Hearing Aids (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 b91f3aa40f16f626b408f0efc9d0b609 and manufactured by INTERTON A/S. The authorized representative in Taiwan is Hongyun Medical Equipment Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INTERTON A/S, 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.