Taiwan FDA registration f36cc4f2db2d5eb02e3d04b212dc0781
"Artini" transilluminator (unsterilized)
TW: "亞堤尼"透照器(未滅菌)
Taiwan·Risk Class 1·ARTINIS MEDICAL SYSTEMS B.V.·Registered Mar 09, 2012 – Mar 09, 2017CancelledRegistration details
- Analysis ID
- f36cc4f2db2d5eb02e3d04b212dc0781
- Customs Code
- DHA04401145700
Company information
- Manufacturer
- ARTINIS MEDICAL SYSTEMS B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- MICROSTAR INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1945 Transilluminator
- Import Information
- import
Dates and status
- Registration Date
- Mar 09, 2012
- Expiry Date
- Mar 09, 2017
- Cancellation Date
- Apr 10, 2017
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Artini" transilluminator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f36cc4f2db2d5eb02e3d04b212dc0781 and manufactured by ARTINIS MEDICAL SYSTEMS B.V.. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS CO., LTD..
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