"Medis" intraocular lens guide (sterilization)
Taiwan·Risk Class 1·MEDICEL AT·Registered Mar 24, 2017 – Mar 24, 2027Active- Analysis ID
- 102cd2075211d62520d41007a8d22a72
- Customs Code
- DHA09401764508
- Manufacturer
- MEDICEL AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Mar 24, 2017
- Expiry Date
- Mar 24, 2027
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Access comprehensive regulatory information for "Medis" intraocular lens 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 102cd2075211d62520d41007a8d22a72 and manufactured by MEDICEL AT. 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 MEDICEL AT, 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.