Taiwan FDA registration 026f900d0afafc32f017bbb77bb1b171
"TOWA" Pupillometer (Non-Sterile)
TW: "投我" 瞳孔計 (未滅菌)
Taiwan·Risk Class 1·MD·TOWA MEDICAL INSTRUMENTS CO., LTD.·Registered Jan 20, 2017 – Jan 20, 2022CancelledRegistration details
- Analysis ID
- 026f900d0afafc32f017bbb77bb1b171
- License Form
- Ministry of Health Medical Device Import No. 017445
- Customs Code
- DHA09401744500
Company information
- Manufacturer
- TOWA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN 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
- Jan 20, 2017
- Expiry Date
- Jan 20, 2022
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "TOWA" 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 026f900d0afafc32f017bbb77bb1b171 and manufactured by TOWA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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