"RODENSTOCK" Corrective Spectacle Lens (Non-sterile)
- Analysis ID
- 3a78dcdd8d0b7bf757aeb5f6f36c9672
- License Form
- Ministry of Health Medical Device Import No. 017565
- Customs Code
- DHA09401756500
- Manufacturer
- RODENSTOCK JAPAN K.K.
- Manufacturer Country
- Japan
- Authorized Representative
- JECKSEN CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Imported from abroad
- Registration Date
- Mar 07, 2017
- Expiry Date
- Mar 07, 2027
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Access comprehensive regulatory information for "RODENSTOCK" Corrective Spectacle Lens (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 3a78dcdd8d0b7bf757aeb5f6f36c9672 and manufactured by RODENSTOCK JAPAN K.K.. The authorized representative in Taiwan is JECKSEN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RODENSTOCK GMBH, RODENSTOCK ASIA LTD., and 3 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.