Taiwan FDA registration 6d58c32d80ec59a2efab93e05a96834e

"RODENSTOCK" Corrective Spectacle Lens (Non-sterile)

TW: "羅敦司得" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RODENSTOCK GMBH·Registered Mar 07, 2017 – Mar 07, 2027Active
Registration details
Analysis ID
6d58c32d80ec59a2efab93e05a96834e
License Form
Ministry of Health Medical Device Import No. 017563
Customs Code
DHA09401756306
Company information
Manufacturer
RODENSTOCK GMBH
Manufacturer Country
Germany
Authorized Representative
JECKSEN CO., LTD.
Product details
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
Dates and status
Registration Date
Mar 07, 2017
Expiry Date
Mar 07, 2027
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About this record

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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