Taiwan FDA registration 26e5262f022dc20d2a6c7e45eaf781ef

"Lianghong" corrective lenses (unsterilized)

TW: "良宏" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Lianghong Optoelectronics Co., Ltd·Registered Jun 01, 2011 – Jun 01, 2016Cancelled
Registration details
Analysis ID
26e5262f022dc20d2a6c7e45eaf781ef
Company information
Manufacturer Country
Taiwan, Province of 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
Domestic
Dates and status
Registration Date
Jun 01, 2011
Expiry Date
Jun 01, 2016
Cancellation Date
Aug 13, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 26e5262f022dc20d2a6c7e45eaf781ef and manufactured by Lianghong Optoelectronics 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 DANYANG HENRY OPTICAL CO., LTD, HANMI SWISS OPTICAL 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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