Taiwan FDA registration 93137ca76767043ed0547fcec6edab60

"RET" Intraocular Lens Guide (Non-Sterile)

TW: "爾易推" 人工水晶體導引器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RET, INC.·Registered Apr 24, 2017 – Apr 24, 2022Expired
Registration details
Analysis ID
93137ca76767043ed0547fcec6edab60
License Form
Ministry of Health Medical Device Import No. 017755
Customs Code
DHA09401775502
Company information
Manufacturer
RET, INC.
Manufacturer Country
Korea, Republic of
Authorized Representative
ICARES MEDICUS, INC.
Product details
Intended Use
Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4300 Intraocular Lens Guide
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 24, 2017
Expiry Date
Apr 24, 2022
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About this record

Access comprehensive regulatory information for "RET" Intraocular Lens Guide (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 93137ca76767043ed0547fcec6edab60 and manufactured by RET, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including R.E.T., INC., and 1 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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