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“Lacrimedics” Dissolvable VisiPlug - Taiwan Registration 7386d1e0d17ae622c66709fb59e7becb

Access comprehensive regulatory information for “Lacrimedics” Dissolvable VisiPlug in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7386d1e0d17ae622c66709fb59e7becb and manufactured by Lacrimedics, Inc.. The authorized representative in Taiwan is Kang Cheng Medical 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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7386d1e0d17ae622c66709fb59e7becb
Registration Details
Taiwan FDA Registration: 7386d1e0d17ae622c66709fb59e7becb
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Device Details

“Lacrimedics” Dissolvable VisiPlug
TW: “拉克美斯”可降解型淚管塞
Risk Class 2
MD

Registration Details

7386d1e0d17ae622c66709fb59e7becb

Ministry of Health Medical Device Import No. 033950

DHA05603395001

Company Information

United States

Product Details

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

M Ophthalmic devices

M9999 Other

Imported from abroad

Dates and Status

Sep 10, 2020

Sep 10, 2025