Taiwan FDA registration 9704fefa1b40d8f181f5ae2b7b304259

"Handong" corrective lenses (unsterilized)

TW: "漢東" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANMI SWISS OPTICAL GLASSES CO., LTD·Registered Dec 02, 2010 – Dec 02, 2015Cancelled
Registration details
Analysis ID
9704fefa1b40d8f181f5ae2b7b304259
Customs Code
DHA04400960701
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
Handong Technology 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
import
Dates and status
Registration Date
Dec 02, 2010
Expiry Date
Dec 02, 2015
Cancellation Date
Aug 09, 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 "Handong" 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 9704fefa1b40d8f181f5ae2b7b304259 and manufactured by HANMI SWISS OPTICAL GLASSES CO., LTD. The authorized representative in Taiwan is Handong Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including Singapore Merchant Mind Optical Co., Ltd. Taiwan Branch, DANYANG TIANMU OPTICAL GLASSES CO., LTD.;; XINXIANG SINWEI TRADING CO., LTD., and 3 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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