Taiwan FDA registration 767f8aa03316e76fa9f6c78616b760b7
"Riester" Medical Examination Light (Non-Sterile)
TW: "瑞司" 醫用檢查燈 (未滅菌)
Taiwan·Risk Class 1·MD·RUDOLF RIESTER GMBH·Registered May 19, 2017 – May 19, 2027ActiveRegistration details
- Analysis ID
- 767f8aa03316e76fa9f6c78616b760b7
- License Form
- Ministry of Health Medical Device Import No. 017860
- Customs Code
- DHA09401786002
Company information
- Manufacturer
- RUDOLF RIESTER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4620 Light source for photofiber dentistry
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 19, 2017
- Expiry Date
- May 19, 2027
About this record
Access comprehensive regulatory information for "Riester" Medical Examination Light (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 767f8aa03316e76fa9f6c78616b760b7 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.
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