Taiwan FDA registration ce6b902c142ee390c4bcd79649f5f4bf

ORIENT Corrective Spectacle Lens (Non-Sterile)

TW: 東方矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·JP OPTICAL PTE LTD.·Registered Feb 08, 2018 – Feb 08, 2023Cancelled
Registration details
Analysis ID
ce6b902c142ee390c4bcd79649f5f4bf
License Form
Ministry of Health Medical Device Manufacturing No. 007106
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Roden Optical Co., Ltd
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5844 corrective lenses
Import Information
Produced in Taiwan, China; Contract manufacturing
Dates and status
Registration Date
Feb 08, 2018
Expiry Date
Feb 08, 2023
Cancellation Date
Oct 20, 2022
Cancellation information
Status
Logged out
Reason
公司歇業
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About this record

Access comprehensive regulatory information for ORIENT 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 ce6b902c142ee390c4bcd79649f5f4bf and manufactured by JP OPTICAL PTE LTD.. The authorized representative in Taiwan is Roden Optical Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including OPTODEV, INC., CHEMIGLAS CORPORATION, and 5 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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