ORIENT Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 8bb9b374389cee83d61dd6262dd5841d
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.
Device Details
Registration Details
8bb9b374389cee83d61dd6262dd5841d
Ministry of Health Medical Device Import No. 017022
DHA09401702201
Product Details
M Ophthalmic devices
M5844 corrective lenses
Imported from abroad
Dates and Status
Sep 22, 2016
Sep 22, 2026
Oct 20, 2022
Cancellation Information
Logged out
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ORIENT Corrective Spectacle Lens (Non-Sterile)
OPTODEV, INC.
c168c6031edb1b2db0b37443da56cafa
1
ORIENT Corrective Spectacle Lens (Non-Sterile)
JP OPTICAL PTE LTD.
ce6b902c142ee390c4bcd79649f5f4bf
1
ORIENT Corrective Spectacle Lens (Non-Sterile)
ESSILOR MANUFACTURING (THAILAND) CO., LTD.
8d0baa6eb106677566fca70bd47ca4f8
1
ORIENT Corrective spectacle lens (Non-Sterile)
CHEMIGLAS CORPORATION
16e6cf8afe4d33394b07cee7baa9c8c3
1
ORIENT Corrective Spectacle Lens (Non-Sterile)
OPTODEV, INC.
d47085e3f727cdbfc996998c436b403c
1

