Taiwan FDA registration a4b2cbfa1b6d1976150677c2e094f78b
“Riester” ri-scope L Ophthalmoscope
TW: “雷伊斯特”直接眼底鏡
Taiwan·Risk Class 2·MD·Rudolf Riester GmbH·Registered Nov 21, 2016 – Nov 21, 2026ActiveRegistration details
- Analysis ID
- a4b2cbfa1b6d1976150677c2e094f78b
- License Form
- Ministry of Health Medical Device Import No. 029115
- Customs Code
- DHA05602911501
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
- Nov 21, 2016
- Expiry Date
- Nov 21, 2026
About this record
Access comprehensive regulatory information for “Riester” ri-scope L Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a4b2cbfa1b6d1976150677c2e094f78b 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. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices