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"Intra-Lock" Capillary Blood Collection Tube (Non-Sterile) - Taiwan Registration a1ebe06bafef5d84a549f789b8e205e1

Access comprehensive regulatory information for "Intra-Lock" Capillary Blood Collection Tube (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 a1ebe06bafef5d84a549f789b8e205e1 and manufactured by INTRA-LOCK, INTERNATIONAL, INC.. The authorized representative in Taiwan is HONG YANG BIOTECHNOLOGY 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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a1ebe06bafef5d84a549f789b8e205e1
Registration Details
Taiwan FDA Registration: a1ebe06bafef5d84a549f789b8e205e1
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Device Details

"Intra-Lock" Capillary Blood Collection Tube (Non-Sterile)
TW: "่‹ฑๅพทๆจ‚ๅฏ" ๆฏ›็ดฐ็ฎก่ก€ๆถฒๆ”ถ้›†็ฎก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

a1ebe06bafef5d84a549f789b8e205e1

Ministry of Health Medical Device Import No. 014581

DHA09401458106

Company Information

United States

Product Details

B Hematology and pathology devices

B6150 Capillary blood collection tube

Imported from abroad

Dates and Status

Oct 16, 2014

Oct 16, 2019

Jul 15, 2022

Cancellation Information

Logged out

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