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Operak tear duct plug - Taiwan Registration 37f143d2e8bd7315abc23f4da92b78ad

Access comprehensive regulatory information for Operak tear duct plug in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37f143d2e8bd7315abc23f4da92b78ad and manufactured by LACRIMEDICS INC.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.

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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37f143d2e8bd7315abc23f4da92b78ad
Registration Details
Taiwan FDA Registration: 37f143d2e8bd7315abc23f4da92b78ad
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Device Details

Operak tear duct plug
TW: ๆญๆฒ›ๆ‹‰ๅ…‹ๆทš็ฎกๅกž
Risk Class 2
Cancelled

Registration Details

37f143d2e8bd7315abc23f4da92b78ad

DHA00601983905

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order.

M Ophthalmology

import

Dates and Status

May 12, 2009

May 12, 2019

May 19, 2022

Cancellation Information

Logged out

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