Taiwan FDA registration e3927c16d2060de0276b9fb8164c156a
"Eddie" manual eye surgery instruments (unsterilized)
TW: “艾迪”手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·ADDITION TECHNOLOGY, INC.·Registered Apr 25, 2008 – Apr 25, 2018CancelledRegistration details
- Analysis ID
- e3927c16d2060de0276b9fb8164c156a
- Customs Code
- DHA04400670101
Company information
- Manufacturer
- ADDITION TECHNOLOGY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- OCARE 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
- Apr 25, 2008
- Expiry Date
- Apr 25, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Eddie" 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 e3927c16d2060de0276b9fb8164c156a and manufactured by ADDITION TECHNOLOGY, INC.. The authorized representative in Taiwan is OCARE LTD..
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