Taiwan FDA registration 8bb9b374389cee83d61dd6262dd5841d

ORIENT Corrective Spectacle Lens (Non-Sterile)

TW: 東方 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·FUJITA OPTICAL CO., LTD.·Registered Sep 22, 2016 – Sep 22, 2026Cancelled
Registration details
Analysis ID
8bb9b374389cee83d61dd6262dd5841d
License Form
Ministry of Health Medical Device Import No. 017022
Customs Code
DHA09401702201
Company information
Manufacturer Country
Japan
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
Sep 22, 2016
Expiry Date
Sep 22, 2026
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 8bb9b374389cee83d61dd6262dd5841d and manufactured by FUJITA OPTICAL CO., 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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