Taiwan FDA registration f4260b64ef4fa1bdc23f48202c8ab513
"Ruisheng" new Japanese automatic corneal curvature refractometer (unsterilized)
TW: “瑞盛”新日本自動角膜弧度驗光機（未滅菌）
Taiwan·Risk Class 1·REXXAM CO., LTD. KAGAWA FACTORY·Registered Sep 14, 2010 – Sep 14, 2015CancelledRegistration details
- Analysis ID
- f4260b64ef4fa1bdc23f48202c8ab513
- Customs Code
- DHA04400919402
Company information
- Manufacturer
- REXXAM CO., LTD. KAGAWA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1760 Automatic Ophthalmic Optical Machine
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 14, 2010
- Expiry Date
- Sep 14, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ruisheng" new Japanese automatic corneal curvature refractometer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4260b64ef4fa1bdc23f48202c8ab513 and manufactured by REXXAM CO., LTD. KAGAWA FACTORY. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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