Nucleic acid detection tube (EDTAK2)
Separation gel / EDTAK2
1、 Scope of application:
It is used to collect venous blood samples for clinical examination. It can be used with disposable venous blood sampling needle or needle holder.
2、 Product performance structure and composition:
This product consists of blood collection tube (glass or pet plastic), butyl rubber plug, PE cap, additive and label.
3、 The dosage of EDTAK2 and EDTAK2 was 0
The amount of separating gel in each tube was 0.5-1.6g, and EDTAK2 in every milliliter of blood was 1.5-2.2mg.
This model and specification product is mainly used for amplification and detection of high-quality clinical nucleic acids (mainly including HBV DNA, HCV and HIV RNA).
After connecting the double needles, turn the blood collection vessel upside down for 5-8 times to make the anticoagulant fully mix with the blood and send it for examination after complete anticoagulation.
L the suction volume of this product is only suitable for clinical use. If the testing institution needs to cooperate with disposable venous blood sampling needle when sampling, and the volume in the hose space should not be filled in advance when testing. In the process of detection and use, the venous blood sampling needle should be pulled out when the sample is collected to the mark of nominal liquid volume and the position of filling line, so as to prevent blood reflux.
L. it is forbidden to use the tube plug due to dislocation and looseness, abnormal additives in the tube, damaged blood collection tube and package or foreign matter in the tube.
Under special circumstances, such as patients with hemorrhagic shock, the amount of blood collected will be affected.
The product should be stored in a clean and well ventilated room with 4-25 ℃, relative humidity less than 80%, no corrosive gas.
This product is only suitable for special altitude areas. In order to achieve accurate blood volume, please order according to your needs.
[production license No.: qsyjxshx No. 20160026
[Registration Certificate No.] qxzz No. 20162410098
[no. of product technical requirements] qxzz No. 20162410098
[name of registrant] Guizhou Tiandi medical device Co., Ltd
[production address] Hongxing Industrial Park, Dingxiao Town, Xingyi City, Qianxinan Buyi and Miao Autonomous Prefecture, Guizhou Province
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