Taiwan FDA registration b7b2291a6e3e970b34befe2ab3161716

"Lianghong" corrective lenses (unsterilized)

TW: "良宏" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DANYANG HENRY OPTICAL CO., LTD·Registered May 07, 2012 – May 07, 2017Cancelled
Registration details
Analysis ID
b7b2291a6e3e970b34befe2ab3161716
Customs Code
DHA04600163301
Company information
Manufacturer Country
China
Authorized Representative
Lianghong Optoelectronics 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 Ophthalmology
Product Type (Level 2)
M.5844 corrective lenses
Import Information
Chinese goods;; input
Dates and status
Registration Date
May 07, 2012
Expiry Date
May 07, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Lianghong" corrective lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b7b2291a6e3e970b34befe2ab3161716 and manufactured by DANYANG HENRY OPTICAL CO., LTD. The authorized representative in Taiwan is Lianghong Optoelectronics Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including HANMI SWISS OPTICAL CO., LTD., Lianghong Optoelectronics 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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