Taiwan FDA registration 3a78dcdd8d0b7bf757aeb5f6f36c9672

"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 JAPAN K.K.·Registered Mar 07, 2017 – Mar 07, 2027Active
Registration details
Analysis ID
3a78dcdd8d0b7bf757aeb5f6f36c9672
License Form
Ministry of Health Medical Device Import No. 017565
Customs Code
DHA09401756500
Company information
Manufacturer Country
Japan
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 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.

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