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Rehm IOL guide (unsterilized) - Taiwan Registration f183f7bfcda51eb0df386e43359d7d0b

Access comprehensive regulatory information for Rehm IOL guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f183f7bfcda51eb0df386e43359d7d0b and manufactured by R.E.T. INC.. The authorized representative in Taiwan is UNITED MEDICAL INC..

This page provides complete technical specifications, regulatory compliance details. 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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f183f7bfcda51eb0df386e43359d7d0b
Registration Details
Taiwan FDA Registration: f183f7bfcda51eb0df386e43359d7d0b
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Device Details

Rehm IOL guide (unsterilized)
TW: โ€œ้Šณๅพทโ€ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

f183f7bfcda51eb0df386e43359d7d0b

DHA04401136301

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 Ophthalmology

M.4300 Artificial crystal body inducer

import

Dates and Status

Feb 10, 2012

Feb 10, 2017

Dec 20, 2019

Cancellation Information

Logged out

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