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FUJI LENS corrective spectacle lens (Non-sterile) - Taiwan Registration de4de111908e8701a52eec60efafc456

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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de4de111908e8701a52eec60efafc456
Registration Details
Taiwan FDA Registration: de4de111908e8701a52eec60efafc456
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Device Details

FUJI LENS corrective spectacle lens (Non-sterile)
TW: ๅฏŒๅ‰ไป• ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

de4de111908e8701a52eec60efafc456

Ministry of Health Medical Device Import No. 015680

DHA09401568000

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

Sep 16, 2015

Sep 16, 2025

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