Taiwan FDA registration c168c6031edb1b2db0b37443da56cafa

ORIENT Corrective Spectacle Lens (Non-Sterile)

TW: 東方矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·OPTODEV, INC.·Registered May 29, 2020 – May 29, 2025Cancelled
Registration details
Analysis ID
c168c6031edb1b2db0b37443da56cafa
License Form
Ministry of Health Medical Device Import No. 021595
Customs Code
DHA09402159508
Company information
Manufacturer
OPTODEV, INC.
Manufacturer Country
Philippines
Authorized Representative
Roden Optical Co., Ltd
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5844 corrective lenses
Import Information
Imported from abroad
Dates and status
Registration Date
May 29, 2020
Expiry Date
May 29, 2025
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 c168c6031edb1b2db0b37443da56cafa and manufactured by OPTODEV, INC.. The authorized representative in Taiwan is Roden Optical Co., Ltd.

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