"Luneau" Corneal Topography (Non-Sterile)
Taiwan·Risk Class 1·MD·LUNEAU TECHNOLOGY OPERATIONS·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- b44ffcc4eb13a65887a54bdff62bb39b
- License Form
- Ministry of Health Medical Device Import Registration No. 015856
- Customs Code
- DHA08401585602
- Manufacturer
- LUNEAU TECHNOLOGY OPERATIONS
- Manufacturer Country
- France
- Authorized Representative
- JUN FENG OPTICAL CO., LTD.
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for "Luneau" Corneal Topography (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b44ffcc4eb13a65887a54bdff62bb39b and manufactured by LUNEAU TECHNOLOGY OPERATIONS. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LUNEAU TECHNOLOGY OPERATIONS, 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.