Test ID: BDIAL
Bleeding Diathesis Profile, Limited
Fees
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
- Authorized users can sign in to the Client Price Portal for detailed fee information.
- Clients without portal access can contact Customer Service 24 hours a day, seven days a week.
- Prospective clients should contact their Regional Manager. For assistance, contact Customer Service.
Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.
NY State Approved
Indicates the status of NY State approval and if the test is orderable for NY State clients.
CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
85240-Coagulation factor VIII assay
85246-von Willebrand factor antigen
85291-Clot solubility factor XIII
85366-Soluble fibrin monomer
85379-D-dimer
85384-Fibrinogen
85390-26-Special coagulation interpretation
85397-von Willebrand factor activity
85610-PT
85670-Thrombin time
85730-APTT
85210-Factor II (if appropriate)
85220-Factor V (if appropriate)
85230-Factor VII (if appropriate)
85245-Ristocetin cofactor (if appropriate)
85247-von Willebrand factor multimer (if appropriate)
85250-Factor IX (If appropriate)
85260-Factor X (if appropriate)
85270-Factor XI (if appropriate)
85280-Factor XII (if appropriate)
85335-Bethesda units (if appropriate)
85335-Factor II inhibitor screen (if appropriate)
85335-Factor V inhibitor screen (if appropriate)
85335-Factor VII inhibitor screen (if appropriate)
85335-Factor VIII inhibitor screen (if appropriate)
85335-Factor IX inhibitor screen (if appropriate)
85335-Factor X inhibitor screen (if appropriate)
85335-Factor XI inhibitor screen (if appropriate)
85410-Alpha-2 plasmin inhibitor (if appropriate)
85597-Platelet neutralization for lupus inhibitor (if appropriate)
85598-Staclot LA (if appropriate)
85611-PT mix 1:1 (if appropriate)
85613-DRVVT (if appropriate)
85613-DRVVT mix (if appropriate)
85613-DRVVT confirm (if appropriate)
85635-Reptilase time (if appropriate)
85732-APTT mix 1:1 (if appropriate)
LOINC® Code Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.
| Result ID | Reporting Name | LOINC Code |
|---|---|---|
| APTTB | Activated Partial Thrombopl Time, P | 14979-9 |
| F8A | Coag Factor VIII Activity Assay, P | 3209-4 |
| FIBC | Fibrinogen, P | 3255-7 |
| 9068 | Factor XIII(13),Scrn | In Process |
| SFM | Soluble Fibrin Monomer | 40702-3 |
| TT | Thrombin Time (Bovine), P | 46717-5 |
| VWAG | von Willebrand Factor Ag, P | 27816-8 |
| VWFX | von Willebrand Factor Activity, P | 68324-3 |
| 7525 | Interpretation | 69049-5 |
| DDMDR | Fibrinogen Equivalent Units (FEU) | In Process |
| PR_TI | Prothrombin Time (PT), P | 5902-2 |
| INR2 | INR | 6301-6 |
| DDIME | D-Dimer Units (DDU) | In Process |
| 7769 | Reviewed by: | N/A |


