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6550-01-574-4440
Imuclone Test Kit
6550015744440 015744440 602
INC: 77777
January 2023
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Test Kit 6550015744440 015744440,602 Imuclone Test Kit 6550015744440 015744440,602 Imuclone Test Kit
6550015744440 015744440,602 Imuclone Test Kit 6550015744440 015744440,602 Imuclone Test Kit 6550-01-
Restrictions 6550-01-574-4440
6550-01-574-4440 is a Imuclone Test Kit that does not have a nuclear hardened feature or any other critical feature such as tolerance, fit restriction or application. Demilitarization of this item has been confirmed and is not currently subject to changes. This item is considered a low risk when released from the control of the Department of Defense. The item may still be subject to the requirements of the Export Administration Regulations (EAR) and the Code of Federal Regulations (CFR). This item may be hazardous as it is in a Federal Supply Class for potentially hazardous items. A MSDS should be available from the supplier for the end user to evaluate any hazards. This item does not contain a precious metal.
End Users 6550-01-574-4440
- Turkey (ZW01)
- Effective Date:
- 1 May 2009
Approved Sources 6550-01-574-4440
- Part Number
- Manufacturer
- Status
- 602
- Manufacturer
- 0PJA0 - American Diagnostica, Inc. (Active)
- Primary Buy
- Primary Buy
Datasheet 6550-01-574-4440
- Characteristic
- Specifications
- FIIG
- Specifications
- A23900
- General Characteristics Item Description [TEXT]
- Measures D-Dimer, Cross Linked Fibrin Degradation Product (Xl-Fdp), In Human Plasma; Elevated Xl-Fdp Levels Indicate Reactive Fibrinolysis And Are Found In A Number Of Arterial And Venous Occlusive Disease States, Including Acute Myocardial Infarction (Mi), Deep Vein Thrombosis (Dvt), Pulmonary Embolisn (Pe) And Disseminated Intravascular Coagulation (Dic); Elevated Xl-Fdp Has Also Been Reported In Surgery, Trauma, Sickle Cell Disease, Liver Disease, Severe Infection, Sepsis, Inflammation, Malignancy And Complications During Pregnancy; Determinations Of Xl-Fdp Levels Have Been Used To Monitor The Course And Response To Thrombolytic Therapy
- Special Features [FEAT]
- Specifications: Samples: Citrate Or Edta Collected Plasma;Precision: Intra-Assay Less Than 10 Percent; Sample Preparation: 1:50 Dilution;Lower Limit Of Detection: 2 Ng/Ml; Assay Time: 2.25 Hours; Standard Range: 0-200 Ng/Ml;Kit Components: 96-Well Antibody Coated Plate,Sample Diluent,D-Dimer Calibrator,High Control Plasma,Low Control Plasma,Detection Antibody,Detection Antibody Diluent,Substrate,Wash Buffer,Stop Solution
- Part Name Assigned By Controlling Agency [CXCY]
- Test Kit, Imuclone D-Dim2179 Er
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Freight Information 6550-01-574-4440
6550-01-574-4440 has freight characteristics managed by Turkey.. 6550-01-574-4440 has a variance between NMFC and UFC when transported by rail and the description should be consulted.