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"AccuVein" Vein Viewing Locator (Non-Sterile) - Taiwan Registration 97e389fbbac7637f6deb95c25114f6c4

Access comprehensive regulatory information for "AccuVein" 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 97e389fbbac7637f6deb95c25114f6c4 and manufactured by ACCUVEIN LLC. The authorized representative in Taiwan is PRO-READY ENTERPRISE 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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97e389fbbac7637f6deb95c25114f6c4
Registration Details
Taiwan FDA Registration: 97e389fbbac7637f6deb95c25114f6c4
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Device Details

"AccuVein" Vein Viewing Locator (Non-Sterile)
TW: "ๆ„›ๅฏ่Šฌ" ้œ่„ˆๅฎšไฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

97e389fbbac7637f6deb95c25114f6c4

Ministry of Health Medical Device Import No. 015007

DHA09401500705

Company Information

United States

Product Details

J General hospital and personal use equipment

J6970 LCD Vein Locator

Imported from abroad

Dates and Status

Mar 17, 2015

Mar 17, 2020

Jun 16, 2022

Cancellation Information

Logged out

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