Taiwan FDA registration dd6b3c8180c8ed047a926bf57b88accb
"Fubi" manual ophthalmic surgical instrument (unsterilized)
TW: "普美" 手動式眼科手術器械 (未滅菌)
Taiwan·Risk Class 1·PRO-MED INSTRUMENTE GMBH·Registered Apr 15, 2006 – Apr 15, 2011CancelledRegistration details
- Analysis ID
- dd6b3c8180c8ed047a926bf57b88accb
- Customs Code
- DHA04400395902
Company information
- Manufacturer
- PRO-MED INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, 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 15, 2006
- Expiry Date
- Apr 15, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fubi" manual ophthalmic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd6b3c8180c8ed047a926bf57b88accb and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, LTD..
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