- Product Name: Pregnancy test Midstream
-
【Common name】 human chorionic gonadotropin (HCG) test strip (colloidal gold immunochromatography)【English name】 Human Chorionic Gonadotropin Test Strip (Colloidal gold immune chromatography)【Product N
型号规格 HCG-D04 1人份/盒
【Common name】 Human chorionic gonadotropin (HCG) test
strip (colloidal gold immunochromatography)
【English】 Human Chorionic Gonadotropin Test Strip
(Colloidal gold immune chromatography)
【Product Name】Pregnancy test midstream 1 test / box
【Main
Composition】
From the test strip and its support composition, test strips on the main
components are:
A) Human chorionic gonadotropin antibody (immobilized on a nitrocellulose membrane);
B) Anti-mouse IgG polyclonal antibody (immobilized on nitrocellulose membrane);
C) Colloidal gold-labeled anti-HCG monoclonal antibody (immobilized on glass
fiber);
D) Other test strip supports.
Other test paper accessories, such as straws, desiccants and so on.
【Storage
conditions and validity】
Stored at 2 to 30 degrees Celsius from dark, self-test qualified from the date
of validity of 36 months, Kaifeng should be used immediately.
【Sample
Requirement】
Any time the urine is suitable for this experiment, in the early stages of
pregnancy, with the morning urine is the best.
【Testing
method】
When using the foil bag will be wrapped along the gap at the torn, remove the
pregnancy test midstream holding the handle end, plum pattern upward,
suction hole down, oblique grip 45 degrees, urine aspiration holes aligned 2-3
seconds , Turn pregnancy test midstream, to continue to grip
pregnant midstream oblique grip, 30 seconds to 5 minutes observed in the
observation window to 5 minutes to interpret shall prevail!
【Manufacturer】
BCT Systems Co., Ltd.
Registration, production Address: 4F & Right side
of 2F, No.3 Lady Road,Fucheng, Longhua , Shenzhen.
Postal
Code: 518110
【Medical
Device Manufacturer License No.】
Guangdong Drug Administration Department
Production Permit No. 20041005
【Medical device registration certificate No.】
Guangdong Device Registration No. 20162401060
【Technical requirements for medical instruments】
Guangdong Device Registration No. 20162401060