Taiwan FDA registration 70159eaf3447cc48d8b5099234366197

"Yongkang" blood collection tube measuring vacuum collection tube

TW: “永康”血沉測定真空採血管

Taiwan·Risk Class 2·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered May 21, 2013 – May 21, 2028Active

Registration details

Analysis ID: 70159eaf3447cc48d8b5099234366197

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 use in clinical laboratories to test red blood cell precipitation rate (ESR).
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1675 Blood collection equipment
Import Information: Domestic

Dates and status

Registration Date: May 21, 2013
Expiry Date: May 21, 2028

About this record

Access comprehensive regulatory information for "Yongkang" blood collection tube measuring vacuum collection tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 70159eaf3447cc48d8b5099234366197 and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..

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