"Riester" Otoscope (Non-Sterile)
- Analysis ID
- 00ef2fa4c6029152a9da3104460f9043
- License Form
- Ministry of Health Medical Device Import No. 015230
- Customs Code
- DHA09401523008
- Manufacturer
- RUDOLF RIESTER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4770 Otoscope
- Import Information
- Imported from abroad
- Registration Date
- May 18, 2015
- Expiry Date
- May 18, 2025
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Access comprehensive regulatory information for "Riester" Otoscope (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 00ef2fa4c6029152a9da3104460f9043 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RUDOLF RIESTER GMBH, and 1 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.