Taiwan FDA registration 09b5a6d3c095ec84ff31e590c89b9727
Rheinland Manual Eye Surgery Instruments (Sterilization)
TW: "萊茵" 手動式眼科手術器械 (滅菌)
Taiwan·Risk Class 1·RHEIN MEDICAL, INC.·Registered Sep 02, 2011 – Sep 02, 2016CancelledRegistration details
- Analysis ID
- 09b5a6d3c095ec84ff31e590c89b9727
- Customs Code
- DHA04401079907
Company information
- Manufacturer
- RHEIN MEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FEDERAL MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 02, 2011
- Expiry Date
- Sep 02, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Rheinland Manual Eye Surgery Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09b5a6d3c095ec84ff31e590c89b9727 and manufactured by RHEIN MEDICAL, INC.. The authorized representative in Taiwan is FEDERAL MEDICAL CO., LTD..
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