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"RET" Intraocular Lens Guide (Non-sterile) - Taiwan Registration bf3e1ba6ed9253dae5963299408436ce

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 bf3e1ba6ed9253dae5963299408436ce and manufactured by R.E.T., INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RET, 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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bf3e1ba6ed9253dae5963299408436ce
Registration Details
Taiwan FDA Registration: bf3e1ba6ed9253dae5963299408436ce
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Device Details

"RET" Intraocular Lens Guide (Non-sterile)
TW: "็‘ž็‰น" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

bf3e1ba6ed9253dae5963299408436ce

Ministry of Health Medical Device Import No. 018549

DHA09401854904

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

Nov 27, 2017

Nov 27, 2022

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