Taiwan FDA registration c9f97d2b1323ffae062311e78307642c
"Shuwei" ophthalmic keratoscopy (unsterilized)
TW: “殊維”眼科角膜鏡 (未滅菌)
Taiwan·Risk Class 1·TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD.·Registered May 17, 2010 – May 17, 2015CancelledRegistration details
- Analysis ID
- c9f97d2b1323ffae062311e78307642c
- Customs Code
- DHA04600093206
Company information
- Manufacturer
- TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- May 17, 2010
- Expiry Date
- May 17, 2015
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Shuwei" ophthalmic keratoscopy (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c9f97d2b1323ffae062311e78307642c and manufactured by TIANJIN SUOWEI ELECTRONIC TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
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