"Dr. Lun" Eye Surgical Perfusion Device (Sterilization)
Taiwan·Risk Class 1·Bausch & Lomb Incorporated·Registered Nov 26, 2019 – Nov 26, 2024Expired- Analysis ID
- 0d1572e86e5849d779ae385e068acce5
- Customs Code
- DHA09402105107
- Manufacturer
- Bausch & Lomb Incorporated
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
- Intended Use
- It is limited to the first level identification scope of ophthalmic surgical perfusion devices (M.4360) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4360 Perfusion device for ophthalmic surgery
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Nov 26, 2019
- Expiry Date
- Nov 26, 2024
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Access comprehensive regulatory information for "Dr. Lun" Eye Surgical Perfusion Device (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d1572e86e5849d779ae385e068acce5 and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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