"RODENSTOCK" Corrective Spectacle Lens (Non-sterile) - Taiwan Registration 3a78dcdd8d0b7bf757aeb5f6f36c9672
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.
Device Details
Registration Details
3a78dcdd8d0b7bf757aeb5f6f36c9672
Ministry of Health Medical Device Import No. 017565
DHA09401756500
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
M Ophthalmic devices
M5844 corrective lenses
Imported from abroad
Dates and Status
Mar 07, 2017
Mar 07, 2027
"RODENSTOCK" Corrective Spectacle Lens (Non-sterile)
RODENSTOCK GMBH
6d58c32d80ec59a2efab93e05a96834e
1
"RODENSTOCK" Corrective Spectacle Lens (Non-sterile)
RODENSTOCK ASIA LTD.
2dc978d6aa64512d990ef064180217e8
1
"Rodenstock" corrective spectacle lens (Non-Sterile)
RODENSTOCK GMBH
148cec58835856bad4a68c114a908e6e
1

