Taiwan FDA registration 554a303698a921b5ecb1f51774cc2bbc

Yijia single-use vacuum blood collection tube (ethylenediaminetetraacetic acid tube)

TW: 醫佳一次性使用真空採血管(乙二胺四乙酸管)

Taiwan·Risk Class 2·HEBEI XINLE SCI&TECH CO., LTD.·Registered May 27, 2014 – May 27, 2019Cancelled

Registration details

Analysis ID: 554a303698a921b5ecb1f51774cc2bbc
Customs Code: DHA09200061303

Company information

Manufacturer: HEBEI XINLE SCI&TECH CO., LTD.
Manufacturer Country: China
Authorized Representative: AGREE HEALTH CARE TECHNOLOGY, LTD.

Product details

Intended Use: It is used for blood routine examination [red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin].
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1675 Blood collection equipment
Import Information: Chinese goods;; input

Dates and status

Registration Date: May 27, 2014
Expiry Date: May 27, 2019
Cancellation Date: Sep 15, 2017

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Yijia single-use vacuum blood collection tube (ethylenediaminetetraacetic acid tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 554a303698a921b5ecb1f51774cc2bbc and manufactured by HEBEI XINLE SCI&TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

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