"Bausch & Len" Ansie can be artificial vitreous
Taiwan·Risk Class 3·LIFECORE BIOMEDICAL, INC.;; BAUSCH & LOMB INCORPORATED·Registered May 11, 2013 – May 11, 2028Active- Analysis ID
- 757eb6ac5b3ac387378171723ca867ea
- Customs Code
- DHA00602502003
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4275 眼內充填用液體
- Import Information
- Contract manufacturing;; input
- Registration Date
- May 11, 2013
- Expiry Date
- May 11, 2028
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Access comprehensive regulatory information for "Bausch & Len" Ansie can be artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 757eb6ac5b3ac387378171723ca867ea and manufactured by LIFECORE BIOMEDICAL, INC.;; BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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