Taiwan FDA registration e250c94309b08bc0463525d04dcb2a3d
“Keeler” Direct Ophthalmoscope
TW: “奇勒”直接眼底鏡
Taiwan·Risk Class 2·MD·KEELER LTD.·Registered Apr 18, 2017 – Apr 18, 2027ActiveRegistration details
- Analysis ID
- e250c94309b08bc0463525d04dcb2a3d
- License Form
- Ministry of Health Medical Device Import No. 029662
- Customs Code
- DHA05602966204
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT INSTRUMENT 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 18, 2017
- Expiry Date
- Apr 18, 2027
About this record
Access comprehensive regulatory information for “Keeler” Direct Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e250c94309b08bc0463525d04dcb2a3d and manufactured by KEELER LTD.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
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