Analyseur d'affinité a1c

L'analyseur d'affinité a1c est un système de détection quantitative basé sur la chromatographie d'affinité au boronate, qui est utilisé avec le kit de test de glycohémoglobine pour détecter le niveau d'hémoglobine a1c (hba1c) dans le sang total humain (sang veineux/piqûre au doigt).

TSH/FT3/FT4 Rapid Quantitative Test (Fluorescence Immunoassay)

The BiotimeTSH/FT3/FT4Rapid Quantitative Test is intended to quantitatively detect the concentration of thyroid-stimulating hormone (TSH), free triiodothyronine (FT3), and free thyroxine (FT4) in human serum and plasma samples on the Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an adjunctive diagnosis of thyroid function. For in vitro diagnostic use only. For professional use only.

Test quantitatif rapide de LH

Lutéinisation L'hormone est une hormone produite par des cellules gonadotropes dans l'hypophyse antérieure GLAND. chez les femmes, une hausse aiguë de LH ("lh Surge") déclencheurs de l'ovulation et du développement du corpus Luteum. chez les hommes, où lh avait également été appelé interstitial cellule-stimulation Hormone (ICSH), il stimule Leydig production cellulaire de testostérone. il agit en synergie avec follicule-stimulant hormone (fsh).

β-hcg Test quantitatif rapide

β-hcg est une immunotasse fluorescente pour la mesure quantitative Du niveau de β-hcg dans le sérum humain et le sang total. Le test est effectué pour aider à diagnostiquer la grossesse si une femme doit subir un traitement médical, et est placée sur certains médicaments ou avoir d'autres tests, tels que les rayons X, qui pourrait nuire au développement bébé.

RF Rapid Quantitative Test (Fluorescence Immunoassay)

The Biotime RF Rapid Quantitative Test is intended to quantify the concentration of RF in human serum, plasma, and whole blood on the Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid in the detection of rheumatoid arthritis. -Fluorescence immunoassay -Rheumatoid arthritis For in vitro diagnostic use only. For professional use only.

HSV-2 IgG/IgM Rapid Test (Fluorescence Immunoassay)

The HSV-2 IgG/IgM Rapid Test is an in vitro immunoassay for the qualitative determination of IgG and IgM class antibodies to HSV2 in human serum. The test is intended for use as an aid in the assessment of immune status and as an aid in the diagnosis of HSV infection. The HSV-2 IgM test shall not be used for prenatal screening of asymptomatic people, and the test results of this reagent shall not be used alone as the basis for termination of pregnancy. -Fluorescent immunoassay -Herpes simplex viruses2 (HSV-2) infection -For in vitro diagnostic use only. For professional use only.

HSV-1 IgG/IgM Rapid Test (Fluorescence Immunoassay)

The HSV-1 IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies to HSV1 in human serum. The test is intended for use as an aid in the assessment of immune status and as an aid in the diagnosis of HSV infection. HSV-1 IgM test shall not be used for prenatal screening of asymptomatic people, and the test results of this reagent shall not be used alone as the basis for termination of pregnancy. -Fluorescent immunoassay -Herpes simplex viruses 1 (HSV-1) infection -For in vitro diagnostic use only. For professional use only.

Toxoplasma IgG/IgM Rapid Test (Fluorescence Immunoassay)

TheToxoplasma IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies toToxoplasma gondii in human serum.IgG results with this assay are used to indicate past or recent infection withToxoplasma gondii. IgM results obtained with this assay are used as an aid in the diagnosis of acute or recentToxoplasma gondii infections. Toxoplasma IgM test shall not be used for prenatal screening of asymptomatic people, and the test results of this reagent shall not be used alone as the basis for termination of pregnancy. -Fluorescent immunoassay -Toxoplasma gondii infection -For in vitro diagnostic use only. For professional use only.

NT-proBNP Rapid Quantitative Test (Chemiluminescence Immunoassay)

NT-proBNP Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the N-terminal pro-B-type natriuretic peptide（NT-proBNP） concentration in human serum, plasma that contains heparin /EDTA and other anticoagulants and venous whole blood samples, mainly used for auxiliary diagnosis of cardiac diseases.

principe	chromatographie d'affinité au boronate
élément d'essai	glycohémoglobine（ hba1c）
taille de l'analyseur	101mmx58mmx25.5mm
poids	84g
temps de test	≤ 3 minutes
transfert de date et connectivité	Bluetooth
alimentation de l'analyseur	batterie lithium-ion 1280mah
stockage de données	500 résultats
c.v.	≤ 3.5 %

Numéro .	éléments
1	r1b
2	r1a
3	puce d'étalonnage
4	R2
5	analyseur d'affinité a1c
6	cartouche d'essai
7	échantillonneur
8	pipette de transfert

Solutions

Solutions au diabète

Analyseur d'affinité A1c

Analyseur d'affinité a1c