Taiwan FDA registration 16e6cf8afe4d33394b07cee7baa9c8c3

ORIENT Corrective spectacle lens (Non-Sterile)

TW: 東方 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·CHEMIGLAS CORPORATION·Registered Nov 25, 2015 – Nov 25, 2020Cancelled
Registration details
Analysis ID
16e6cf8afe4d33394b07cee7baa9c8c3
License Form
Ministry of Health Medical Device Import No. 015897
Customs Code
DHA09401589702
Company information
Manufacturer Country
Korea, Republic of
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
Nov 25, 2015
Expiry Date
Nov 25, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 16e6cf8afe4d33394b07cee7baa9c8c3 and manufactured by CHEMIGLAS CORPORATION. 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., FUJITA OPTICAL CO., LTD., 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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