Taiwan FDA registration 8d0baa6eb106677566fca70bd47ca4f8

ORIENT Corrective Spectacle Lens (Non-Sterile)

TW: 東方 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ESSILOR MANUFACTURING (THAILAND) CO., LTD.·Registered Jun 07, 2016 – Jun 07, 2021Cancelled
Registration details
Analysis ID
8d0baa6eb106677566fca70bd47ca4f8
License Form
Ministry of Health Medical Device Import No. 016633
Customs Code
DHA09401663309
Company information
Manufacturer Country
Thailand
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
Jun 07, 2016
Expiry Date
Jun 07, 2021
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 8d0baa6eb106677566fca70bd47ca4f8 and manufactured by ESSILOR MANUFACTURING (THAILAND) 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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