"Bausch & Len" IOL Guide (Sterilization)
Taiwan·Risk Class 1·BAUSCH & LOMB INC.·Registered Dec 25, 2009 – Dec 25, 2019Cancelled- Analysis ID
- ae9ce298dae1d7bc35a1ac90e31cfc65
- Customs Code
- DHA04400842309
- Manufacturer
- BAUSCH & LOMB INC.
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- Input;; QMS/QSD
- Registration Date
- Dec 25, 2009
- Expiry Date
- Dec 25, 2019
- Cancellation Date
- May 19, 2022
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Bausch & Len" IOL Guide (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae9ce298dae1d7bc35a1ac90e31cfc65 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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