Hangzhou Dalton BioSciences, Ltd.

Zhejiang,China

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Hangzhou Dalton BioSciences, Ltd.

Zhejiang,China

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Hangzhou Dalton BioSciences, Ltd.

Zhejiang,China

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High Risk Human Papillomavirus (HPV) Genotyping System

FOB Price : Get a Price/Quote

Min.Order : 2000 Piece(s)

Certification : CFDA,CE,MDSAP

Brand Name : DALTONbio

Payment Terms : T/T

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product information

brand name : DALTONbio
certification : CFDA,CE,MDSAP
min.order : 2000 Piece(s)
warranty : 24 months
payment terms : T/T
Packaging : 48 tests/kit, 96 tests/kit
Specification : 16×13×12 cm
place of origin : China

product description

[Product Components]
Automatic Hybrid Capture System (HB-104C\ HB-304C)
Chemiluminescence Immunoassay Analyzer (CS-SA301C)
96 well Hybridization microplate with lid
Specimen collection tube screw caps
Disposable cervical sampling brush
Specimen Preservation Solution
Cell Preservation Solution
Antigen Retrieval Buffer
Wash Buffer

The DH3 is an in vitro nucleic hybridization assay, using a new generation hybrid capture technology for the qualitative detection of 14 high-risk types of human papillomavirus (HPV) in cervical specimens. The HPV types detected by the assay are the high-risk HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68. The DH3 can distinguish between HPV16/18 and the other 12 pooled HR-HPV genotypes. The test can be used for one of the following indications:
1. The test can be used for patients with ASC-US (atypical squamous cells of undetermined significance) cervical cytology results to assess the presence or absence of high-risk HPV types. This information may be used to determine the need for referral to colposcopy. The results of this test are not intended to prevent women from proceeding to colposcopy.
2. The test can be used with Pap to adjunctively screen to assess the presence or absence of high-risk HPV types. This information, together with the physician's assessment of cytology history, other risk factors, and professional guidelines, may be used to guide patient management.
3. The test can be used as a first-line primary cervical cancer screening test to detect high risk HPV. Women who test negative for high-risk HPV types by this test should be followed in accordance with the physician's assessment of screening and medical history, other risk factors, and professional guidelines. Women who test positive for HPV 16/18 should be referred to colposcopy. Women who test high-risk HPV positive and HPV 16/18 negative by the test (indicating a positive for the other 12 high risk HPV types) should be evaluated by cervical cytology to determine the need for referral to colposcopy.

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