Taiwan FDA registration 86895bcf9d27367f7a73d8b3c3269211

Optovision Corrective Spectacle Lens(Non-Sterile)

TW: 歐特 矯正鏡片(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·OptoVision GERMANY·Registered Feb 10, 2020 – Feb 10, 2025Expired
Registration details
Analysis ID
86895bcf9d27367f7a73d8b3c3269211
License Form
Ministry of Health Medical Device Import No. 021243
Customs Code
DHA09402124303
Company information
Manufacturer
OptoVision GERMANY
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
Feb 10, 2020
Expiry Date
Feb 10, 2025
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About this record

Access comprehensive regulatory information for Optovision 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 86895bcf9d27367f7a73d8b3c3269211 and manufactured by OptoVision GERMANY. 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 HONG KONG OPTICAL LENS 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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