Taiwan FDA registration 47fea77c427e095427aeeeceb3cd3807
"Luneau" Pupillometer (Non-Sterile)
TW: "路尼耳" 瞳孔計 (未滅菌)
Taiwan·Risk Class 1·MD·LUNEAU TECHNOLOGY OPERATIONS·Registered Apr 20, 2017 – Apr 20, 2022CancelledRegistration details
- Analysis ID
- 47fea77c427e095427aeeeceb3cd3807
- License Form
- Ministry of Health Medical Device Import No. 017742
- Customs Code
- DHA09401774206
Company information
- Manufacturer
- LUNEAU TECHNOLOGY OPERATIONS
- Manufacturer Country
- France
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1700 Pupillometer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2017
- Expiry Date
- Apr 20, 2022
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Luneau" Pupillometer (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 47fea77c427e095427aeeeceb3cd3807 and manufactured by LUNEAU TECHNOLOGY OPERATIONS. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
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