"Dr. Lun" Eye Surgical Perfusion Device (Sterilization)
Taiwan·Risk Class 1·BIEFFE MEDITAL S. P. A.·Registered Jul 19, 2018 – Jul 19, 2028Active- Analysis ID
- 360698f6903275ede920ce849d3c456f
- Customs Code
- DHA09401933006
- Manufacturer
- BIEFFE MEDITAL S. P. A.
- Manufacturer Country
- Italy
- 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
- Jul 19, 2018
- Expiry Date
- Jul 19, 2028
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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 360698f6903275ede920ce849d3c456f and manufactured by BIEFFE MEDITAL S. P. A.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Bausch & Lomb Incorporated, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.