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"Neotech" Vein Viewing Locator (Non-Sterile) - Taiwan Registration 82dc20519a2445ac27bd3d2d1bac7581

Access comprehensive regulatory information for "Neotech" Vein Viewing Locator (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 82dc20519a2445ac27bd3d2d1bac7581 and manufactured by NEOTECH PRODUCTS LLC. The authorized representative in Taiwan is CHAMP MEDICS 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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82dc20519a2445ac27bd3d2d1bac7581
Registration Details
Taiwan FDA Registration: 82dc20519a2445ac27bd3d2d1bac7581
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Device Details

"Neotech" Vein Viewing Locator (Non-Sterile)
TW: "ๅฆฎ็ˆพๆณฐๅ…‹" ้œ่„ˆๅฎšไฝๅ™จ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
MD

Registration Details

82dc20519a2445ac27bd3d2d1bac7581

Ministry of Health Medical Device Import No. 019823

DHA09401982303

Company Information

United States

Product Details

Limited to the first level identification range of the "liquid crystal vein locator (J.6970)" of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J6970 LCD Vein Locator

Imported from abroad

Dates and Status

Nov 15, 2018

Nov 15, 2028