Taiwan FDA registration 1b2ab5b40e01896f1876881678f5ef5f
"Sight Wonder" corneal knife (unsterilized)
TW: "視萬得" 角膜刀 (未滅菌)
Taiwan·Risk Class 1·SCHWIND EYE-TECH-SOLUTIONS GMBH·Registered Oct 04, 2010 – Oct 04, 2020CancelledRegistration details
- Analysis ID
- 1b2ab5b40e01896f1876881678f5ef5f
- Customs Code
- DHA04400930406
Company information
- Manufacturer
- SCHWIND EYE-TECH-SOLUTIONS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Limited to the first level identification range of the "corneal knife (M.4370)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4370 Corneal knife
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2010
- Expiry Date
- Oct 04, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Sight Wonder" corneal knife (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b2ab5b40e01896f1876881678f5ef5f and manufactured by SCHWIND EYE-TECH-SOLUTIONS GMBH. The authorized representative in Taiwan is CLINICO INC..
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