Taiwan FDA registration 06d3717f50afaaa7d73ce022042d4b3b

Apollo lens corrective spectacle lens (Non-sterile)

TW: 至尊 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RODENSTOCK GMBH·Registered Sep 24, 2015 – Sep 24, 2025Expired
Registration details
Analysis ID
06d3717f50afaaa7d73ce022042d4b3b
License Form
Ministry of Health Medical Device Import No. 015696
Customs Code
DHA09401569602
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 24, 2015
Expiry Date
Sep 24, 2025
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About this record

Access comprehensive regulatory information for Apollo 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 06d3717f50afaaa7d73ce022042d4b3b 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, 2 companies making similar products including FUJITA OPTICAL CO., LTD., HONG KONG OPTICAL LENS CO., LTD., and 2 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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