Taiwan FDA registration 662098781e099286f5baa785afbf49ed
"Rheinland" Manual Eye Surgery Instruments (Unsterilized)
TW: "萊茵" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·RHEIN MEDICAL INC.·Registered Mar 14, 2011 – Mar 14, 2016CancelledRegistration details
- Analysis ID
- 662098781e099286f5baa785afbf49ed
- Customs Code
- DHA04401001206
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
- import
Dates and status
- Registration Date
- Mar 14, 2011
- Expiry Date
- Mar 14, 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 (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 662098781e099286f5baa785afbf49ed and manufactured by RHEIN MEDICAL INC.. The authorized representative in Taiwan is FEDERAL MEDICAL CO., LTD..
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