Taiwan FDA registration 34dd88798bbd76ed8aa7c6654e916d8e
"Reist" battery-powered retinal scope (unsterilized)
TW: "雷伊斯特" 電池供電式視網膜鏡 (未滅菌)
Taiwan·Risk Class 1·Rudolf Riester GmbH·Registered Dec 24, 2019 – Dec 24, 2029ActiveRegistration details
- Analysis ID
- 34dd88798bbd76ed8aa7c6654e916d8e
- Customs Code
- DHA09402113003
Company information
- Manufacturer
- Rudolf Riester GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Retinal Scope (M.1780) First Grade Identification Range.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1780 Retinal Lens
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 24, 2019
- Expiry Date
- Dec 24, 2029
About this record
Access comprehensive regulatory information for "Reist" battery-powered retinal scope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 34dd88798bbd76ed8aa7c6654e916d8e and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
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