Taiwan FDA registration de4de111908e8701a52eec60efafc456

FUJI LENS corrective spectacle lens (Non-sterile)

TW: 富吉仕 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RODENSTOCK GMBH·Registered Sep 16, 2015 – Sep 16, 2025Expired
Registration details
Analysis ID
de4de111908e8701a52eec60efafc456
License Form
Ministry of Health Medical Device Import No. 015680
Customs Code
DHA09401568000
Company information
Manufacturer
RODENSTOCK GMBH
Manufacturer Country
Germany
Authorized Representative
HKO OPTICAL LENS (TAIWAN) 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
Sep 16, 2015
Expiry Date
Sep 16, 2025
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About this record

Access comprehensive regulatory information for FUJI LENS 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 de4de111908e8701a52eec60efafc456 and manufactured by RODENSTOCK GMBH. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ASAHI LITE OPTICAL CO., LTD., and 1 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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