Taiwan FDA registration dbf3d7e7fcce57740b3b35f5fcb433e3

"Lianghiro" corrective lenses (unsterilized)

TW: 〝良宏〞矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DANYANG KANGWEI OPTICALI CO.,LTD·Registered Apr 13, 2012 – Apr 13, 2017Cancelled
Registration details
Analysis ID
dbf3d7e7fcce57740b3b35f5fcb433e3
Customs Code
DHA04600162301
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
Input;; Chinese goods
Dates and status
Registration Date
Apr 13, 2012
Expiry Date
Apr 13, 2017
Cancellation Date
Jan 06, 2020
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 "Lianghiro" 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 dbf3d7e7fcce57740b3b35f5fcb433e3 and manufactured by DANYANG KANGWEI OPTICALI CO.,LTD. The authorized representative in Taiwan is Lianghong Optoelectronics Co., Ltd.

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