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"RODENSTOCK" Corrective Spectacle Lens (Non-sterile) - Taiwan Registration 6d58c32d80ec59a2efab93e05a96834e

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 6d58c32d80ec59a2efab93e05a96834e and manufactured by RODENSTOCK GMBH. The authorized representative in Taiwan is JECKSEN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 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.

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6d58c32d80ec59a2efab93e05a96834e
Registration Details
Taiwan FDA Registration: 6d58c32d80ec59a2efab93e05a96834e
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Device Details

"RODENSTOCK" Corrective Spectacle Lens (Non-sterile)
TW: "็พ…ๆ•ฆๅธๅพ—" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6d58c32d80ec59a2efab93e05a96834e

Ministry of Health Medical Device Import No. 017563

DHA09401756306

Company Information

Germany

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

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