Taiwan FDA registration 097f8ab0819fc8fbac80354bfc0b5bff
"Zeiss" full femtosecond laser corneal instrument
TW: “蔡司” 全飛秒雷射角膜儀
Taiwan·Risk Class 2·CARL ZEISS MEDITEC AG·Registered May 09, 2022 – May 09, 2027ActiveRegistration details
- Analysis ID
- 097f8ab0819fc8fbac80354bfc0b5bff
- Customs Code
- DHA05603542604
Company information
- Manufacturer
- CARL ZEISS MEDITEC AG
- Manufacturer Country
- Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- May 09, 2022
- Expiry Date
- May 09, 2027
About this record
Access comprehensive regulatory information for "Zeiss" full femtosecond laser corneal instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 097f8ab0819fc8fbac80354bfc0b5bff and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
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