Taiwan FDA registration da8742d00ff2741fc10c155866337f20
"Zeiss" excimer laser and accessories
TW: “蔡司”準分子雷射儀及配件
Taiwan·Risk Class 3·CARL ZEISS MEDITEC AG·Registered Aug 06, 2014 – Aug 06, 2024ExpiredRegistration details
- Analysis ID
- da8742d00ff2741fc10c155866337f20
- Customs Code
- DHA05602642501
Company information
- Manufacturer
- CARL ZEISS MEDITEC AG
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.0001 眼科用準分子雷射系統
- Import Information
- import
Dates and status
- Registration Date
- Aug 06, 2014
- Expiry Date
- Aug 06, 2024
About this record
Access comprehensive regulatory information for "Zeiss" excimer laser and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number da8742d00ff2741fc10c155866337f20 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..
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