Taiwan FDA registration 6d72caaf116f270b4e54bea8afc832ed
"Vivilla" corneal map analyzer (unsterilized)
TW: “威微賴”角膜地圖分析儀 (未滅菌)
Taiwan·Risk Class 1·WAVELIGHT GMBH·Registered Apr 13, 2010 – Apr 13, 2015CancelledRegistration details
- Analysis ID
- 6d72caaf116f270b4e54bea8afc832ed
- Customs Code
- DHA04400871203
Company information
- Manufacturer
- WAVELIGHT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
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
- import
Dates and status
- Registration Date
- Apr 13, 2010
- Expiry Date
- Apr 13, 2015
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Vivilla" corneal map analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6d72caaf116f270b4e54bea8afc832ed and manufactured by WAVELIGHT GMBH. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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