Taiwan FDA registration 4ed7077637f1a6fc97abee8959141133
“Riester” Indirect Ophthalmoscope
TW: “雷伊斯特”間接眼底鏡
Taiwan·Risk Class 2·MD·Rudolf Riester GmbH·Registered Apr 27, 2022 – May 25, 2027ActiveRegistration details
- Analysis ID
- 4ed7077637f1a6fc97abee8959141133
- License Form
- Ministry of Health Medical Device Import No. 029769
- Customs Code
- DHA05602976909
Company information
- Manufacturer
- Rudolf Riester GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1570 fundus mirror
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 27, 2022
- Expiry Date
- May 25, 2027
About this record
Access comprehensive regulatory information for “Riester” Indirect Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ed7077637f1a6fc97abee8959141133 and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
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