"Gulden" Ophthalmic Bar Prism (Non-Sterile)
Taiwan·Risk Class 1·MD·GULDEN OPHTHALMICS·Registered Oct 03, 2017 – Oct 03, 2027Active- Analysis ID
- cef54a5624e67610df72fabcb845a2b8
- License Form
- Ministry of Health Medical Device Import No. 018375
- Customs Code
- DHA09401837500
- Manufacturer
- GULDEN OPHTHALMICS
- Manufacturer Country
- United States
- Authorized Representative
- FORESIGHT ASSISTIVE TECHNOLOGY INC.
- Intended Use
- Limited to the first level recognition range of rod prism (M.1650) for ophthalmology under the management measures for medical equipment.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1650 Rod prism for ophthalmology
- Import Information
- Imported from abroad
- Registration Date
- Oct 03, 2017
- Expiry Date
- Oct 03, 2027
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Access comprehensive regulatory information for "Gulden" Ophthalmic Bar Prism (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 cef54a5624e67610df72fabcb845a2b8 and manufactured by GULDEN OPHTHALMICS. The authorized representative in Taiwan is FORESIGHT ASSISTIVE TECHNOLOGY INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GULDEN OPHTHALMICS, 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.