Taiwan FDA registration d47085e3f727cdbfc996998c436b403c

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 Jan 09, 2015 – Jan 09, 2020Cancelled
Registration details
Analysis ID
d47085e3f727cdbfc996998c436b403c
License Form
Ministry of Health Medical Device Import No. 014834
Customs Code
DHA09401483409
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
Jan 09, 2015
Expiry Date
Jan 09, 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 d47085e3f727cdbfc996998c436b403c 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 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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