Taiwan FDA registration 94ea36582b7ca9ffd735ce6871aff454
"Dr. Lun" Anshia Eye Surgical Perfusion Device (Sterilized)
TW: “博士倫” 安視亞眼睛手術灌注裝置(滅菌)
Taiwan·Risk Class 1·BAUSCH & LOMB IRELAND·Registered Dec 14, 2011 – Dec 14, 2016CancelledRegistration details
- Analysis ID
- 94ea36582b7ca9ffd735ce6871aff454
- Customs Code
- DHA04401118006
Company information
- Manufacturer
- BAUSCH & LOMB IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Eye Surgical Perfusion Device (M.4360)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4360 Perfusion device for ophthalmic surgery
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 14, 2011
- Expiry Date
- Dec 14, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Dr. Lun" Anshia Eye Surgical Perfusion Device (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 94ea36582b7ca9ffd735ce6871aff454 and manufactured by BAUSCH & LOMB IRELAND. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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