Taiwan FDA registration b0223555d375df3309d0bf2073af3c5e
"Medis" Microjet IOL Guide (Sterilization)
TW: “麥迪斯”微可捷人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·MEDICEL AT·Registered Jul 14, 2009 – Jul 14, 2019CancelledRegistration details
- Analysis ID
- b0223555d375df3309d0bf2073af3c5e
- Customs Code
- DHA04400790601
Company information
- Manufacturer
- MEDICEL AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- 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
Dates and status
- Registration Date
- Jul 14, 2009
- Expiry Date
- Jul 14, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medis" Microjet 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 b0223555d375df3309d0bf2073af3c5e and manufactured by MEDICEL AT. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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