Taiwan FDA registration 79e6a27d189878b468ce22b93b6f6c5c
Opto Ophthalmic Double Frequency Chrome Ya Chrome Laser
TW: 澳普拓眼科雙倍頻銣雅鉻雷射
Taiwan·Risk Class 2·LIGHTMED CORPORATION·Registered Apr 02, 2007 – Oct 30, 2016CancelledRegistration details
- Analysis ID
- 79e6a27d189878b468ce22b93b6f6c5c
- Customs Code
- DHY00500215702
Company information
- Manufacturer
- LIGHTMED CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LIGHTMED CORPORATION
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.4390 眼科雷射裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 02, 2007
- Expiry Date
- Oct 30, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Opto Ophthalmic Double Frequency Chrome Ya Chrome Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79e6a27d189878b468ce22b93b6f6c5c and manufactured by LIGHTMED CORPORATION. The authorized representative in Taiwan is LIGHTMED CORPORATION.
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