Taiwan FDA registration aa3550acdcb1eeb0d03a5f1a8f700242

Corrective lenses according to the vision path (unsterilized)

TW: 依視路 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·ESSILOR INTERNATIONAL (COMPAGINE GENERALE D'OPTIQUE);;OPTODEV, INC.·Registered Nov 05, 2010 – Nov 05, 2020Cancelled
Registration details
Analysis ID
aa3550acdcb1eeb0d03a5f1a8f700242
Customs Code
DHA04400946201
Company information
Manufacturer Country
Philippines;;France
Authorized Representative
ESSILOR-POLYLITE TAIWAN CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5844 corrective lenses
Import Information
import
Dates and status
Registration Date
Nov 05, 2010
Expiry Date
Nov 05, 2020
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for Corrective lenses according to the vision path (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aa3550acdcb1eeb0d03a5f1a8f700242 and manufactured by ESSILOR INTERNATIONAL (COMPAGINE GENERALE D'OPTIQUE);;OPTODEV, INC.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including ESSILOR-POLYLITE TAIWAN CO., LTD., CHEMIGLAS CORPORATION, and 3 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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