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"RET" Intraocular Lens Guide (Non-Sterile) - Taiwan Registration 93137ca76767043ed0547fcec6edab60

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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93137ca76767043ed0547fcec6edab60
Registration Details
Taiwan FDA Registration: 93137ca76767043ed0547fcec6edab60
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Device Details

"RET" Intraocular Lens Guide (Non-Sterile)
TW: "็ˆพๆ˜“ๆŽจ" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

93137ca76767043ed0547fcec6edab60

Ministry of Health Medical Device Import No. 017755

DHA09401775502

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.

M Ophthalmic devices

M4300 Intraocular Lens Guide

Imported from abroad

Dates and Status

Apr 24, 2017

Apr 24, 2022

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