DEVICE: REAADS von Willebrand Factor Activity Test Kit (00855360006267)
Device Identifier (DI) Information
REAADS von Willebrand Factor Activity Test Kit
10826
In Commercial Distribution
10826
CORGENIX MEDICAL CORPORATION
10826
In Commercial Distribution
10826
CORGENIX MEDICAL CORPORATION
INTENDED USE
An enzyme-linked immunosorbent assay (ELISA) for the quantitative determination of Von Willebrand Factor Activity (VWF:Act) in citrated human plasma. For In Vitro Diagnostic Use.
SUMMARY OF THE TEST
Von Willebrand Factor Antigen (VWF:Ag or Factor VIII-related protein) is a plasma protein found in circulation combined by non-covalent interactions with Factor VIII (FVIII:C), a pro-coagulant protein also known as the anti-hemophilic factor. Deficiency of FVIII causes classic hemophilia while deficiency of VWF causes von Willebrand disease. Von Willebrand Disease is characterized by a deficiency or defect of VWF. Greater than 70% of Von Willebrand disease patients have a type 1 deficiency while approximately 20% have a type II deficiency. The laboratory diagnosis of Von Willebrand disease may require both quantitative and qualitative (functional) determinations to differentiate the two predominant subtypes of the disease, type I and type II. The classification of Von Willebrand disease into subtypes is important in determining the course of clinical treatment.
PRINCIPLE OF THE TEST
The REAADS VWF:Act assay is a sandwich ELISA. A monoclonal capture antibody specific for the portion of VWF which binds platelets is coated to 96-microwell polystyrene plates. Diluted patient plasma is incubated in the wells. The plates are washed to remove unbound proteins and other plasma molecules. Bound antigen is quantitated using horseradish peroxidase (HRP) conjugated anti-human VWF detection antibody. Following incubation, unbound conjugate is removed by washing. A chromogenic substrate of tetramethylbenzidine (TMB) and hydrogen peroxide (H2O2) is added to develop a colored reaction. The intensity of the color is measured in O.D. units with a spectrophotometer at 450 nm. Patient VWF:Act in relative percent concentration is determined against a curve made from the reference plasma provided with the kit. Refer to Product Package Insert.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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62152 | von Willebrand factor:glycoprotein Ib binding activity (vWF:GPIb) IVD, kit, enzyme immunoassay (EIA) |
A collection of reagents and other associated materials intended to be used for the quantitative measurement of von Willebrand factor:glycoprotein Ib binding activity (vWF:GPIb) in a clinical specimen, using an enzyme immunoassay (EIA) method.
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FDA Product Code
[?]Product Code | Product Code Name |
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GGP | Test, Qualitative And Quantitative Factor Deficiency |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K032139 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Storage Environment Temperature: between 2 and 8 Degrees Celsius |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
09cb21ea-2fc6-4b41-8db0-b02c9dc61e38
July 06, 2018
3
July 14, 2016
July 06, 2018
3
July 14, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
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Secondary DI
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
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CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
1-800-729-5661
technicalsupport@corgenix.com
technicalsupport@corgenix.com