Taiwan FDA registration b57e0cd3a289c490bee500911df5da9f

TEOS Corrective Spectacle Lens (Non-Sterile)

TW: TEOS 矯正鏡片(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HWA MEEI OPTICAL CO., LTD.·Registered Feb 02, 2016 – Feb 02, 2026Expired
Registration details
Analysis ID
b57e0cd3a289c490bee500911df5da9f
License Form
Ministry of Health Medical Device Manufacturing No. 006045
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
HWA MEEI OPTICAL 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
Produced in Taiwan, China
Dates and status
Registration Date
Feb 02, 2016
Expiry Date
Feb 02, 2026
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About this record

Access comprehensive regulatory information for TEOS 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 b57e0cd3a289c490bee500911df5da9f and manufactured by HWA MEEI OPTICAL CO., LTD.. The authorized representative in Taiwan is HWA MEEI OPTICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HWA MEEI 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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