Taiwan FDA registration 141abe05435408acc786a8dc6809ae6a

Medical single-use non-vacuum blood collection tubes (tripotassium ethylenediaminetetraacetate)

TW: 醫凡一次性使用非真空採血管(乙二胺四乙酸三鉀)

Taiwan·Risk Class 2·HEBEI XINLE SCI & TECH CO., LTD.·Registered May 12, 2014 – May 12, 2029Active

Registration details

Analysis ID: 141abe05435408acc786a8dc6809ae6a
Customs Code: DHA09200052901

Company information

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

Product details

Intended Use: This product is used for routine blood [red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin] examination.
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 12, 2014
Expiry Date: May 12, 2029

About this record

Access comprehensive regulatory information for Medical single-use non-vacuum blood collection tubes (tripotassium ethylenediaminetetraacetate) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 141abe05435408acc786a8dc6809ae6a and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

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