Taiwan FDA registration cfa96e2f8fb942a44bb41dfdd2866b8a

CRX TEOS Corrective Spectacle Lens (Non-Sterile)

TW: CRX TEOS 矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·HWA MEEI OPTICAL CO., LTD.·Registered Jun 29, 2016 – Jun 29, 2026Expired

Registration details

Analysis ID: cfa96e2f8fb942a44bb41dfdd2866b8a
License Form: Ministry of Health Medical Device Manufacturing No. 006257

Company information

Manufacturer: HWA MEEI OPTICAL CO., LTD.
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: Jun 29, 2016
Expiry Date: Jun 29, 2026

About this record

Access comprehensive regulatory information for CRX 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 cfa96e2f8fb942a44bb41dfdd2866b8a and manufactured by HWA MEEI OPTICAL CO., LTD.. The authorized representative in Taiwan is HWA MEEI OPTICAL CO., LTD..

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