Taiwan FDA registration 531141dbbc3a94ae9ff558c7b078abfa
"SHIE-TUNG" REFRACTOR (Non-Sterile)
TW: "協同" 自覺式驗光儀 (未滅菌)
Taiwan·Risk Class 1·MD·TOWA MEDICAL INSTRUMENTS CO., LTD.·Registered Aug 28, 2015 – Aug 28, 2020CancelledRegistration details
- Analysis ID
- 531141dbbc3a94ae9ff558c7b078abfa
- License Form
- Ministry of Health Medical Device Import No. 015614
- Customs Code
- DHA09401561400
Company information
- Manufacturer
- TOWA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Synergy Optics Ltd
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1770 Manual Fold Meter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 28, 2015
- Expiry Date
- Aug 28, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "SHIE-TUNG" REFRACTOR (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 531141dbbc3a94ae9ff558c7b078abfa and manufactured by TOWA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Synergy Optics Ltd.
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