"Interton" Hearing Aids (Non-Sterile)
Taiwan·Risk Class 1·MD·INTERTON A/S·Registered Dec 18, 2015 – Dec 18, 2025Expired- Analysis ID
- d1e757592a5aea7fe83358ecb303b537
- License Form
- Ministry of Health Medical Device Import No. 015993
- Customs Code
- DHA09401599308
- Manufacturer
- INTERTON A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- TAIWAN VAPOR CORPORATION
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
- Registration Date
- Dec 18, 2015
- Expiry Date
- Dec 18, 2025
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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 d1e757592a5aea7fe83358ecb303b537 and manufactured by INTERTON A/S. The authorized representative in Taiwan is TAIWAN VAPOR CORPORATION.
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.