Taiwan FDA registration 910147466ece165fac33ff3a36a64af5

VACUKANG Non-Additive Blood Collection Tubes.

TW: “永康” 無添加真空採血管

Taiwan·Risk Class 2·MD·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered May 21, 2015 – May 21, 2025Expired

Registration details

Analysis ID: 910147466ece165fac33ff3a36a64af5
License Form: Ministry of Health Medical Device Manufacturing No. 004931

Company information

Manufacturer: YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.

Product details

Intended Use: It is used to collect blood for clinical laboratory testing, serum or whole blood.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1675 Blood Sample Collection Device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 21, 2015
Expiry Date: May 21, 2025

About this record

Access comprehensive regulatory information for VACUKANG Non-Additive Blood Collection Tubes. in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 910147466ece165fac33ff3a36a64af5 and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE 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.