Taiwan FDA registration 093990f1e1fe2c869593b03e1f77bcde
Feist superimposed astigmatism crystals
TW: 飛斯特疊加散光水晶體
Registration details
- Analysis ID
- 093990f1e1fe2c869593b03e1f77bcde
- Customs Code
- DHA05603513200
Company information
- Manufacturer
- 1st Q GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- CRYSTALVISION CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- import
Dates and status
- Registration Date
- Jan 17, 2022
- Expiry Date
- Jan 17, 2027
About this record
Access comprehensive regulatory information for Feist superimposed astigmatism crystals in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 093990f1e1fe2c869593b03e1f77bcde and manufactured by 1st Q GmbH. The authorized representative in Taiwan is CRYSTALVISION CO., LTD..
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