Taiwan FDA registration 6b819966d4b64631253a41cd354b0885
"Meridian" ophthalmic chrome chromium laser
TW: “美利迪恩” 眼科銣雅鉻雷射
Taiwan·Risk Class 2·MERIDIAN AG·Registered May 15, 2008 – May 15, 2023ExpiredRegistration details
- Analysis ID
- 6b819966d4b64631253a41cd354b0885
- Customs Code
- DHA00601886106
Company information
- Manufacturer
- MERIDIAN AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- EVERLIGHT 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.4392 後囊切除用Nd:YAG雷射
- Import Information
- import
Dates and status
- Registration Date
- May 15, 2008
- Expiry Date
- May 15, 2023
About this record
Access comprehensive regulatory information for "Meridian" ophthalmic chrome chromium laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b819966d4b64631253a41cd354b0885 and manufactured by MERIDIAN AG. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
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