FDA UDI In Commercial Distribution 🇺🇸 United States

LeukoStrat

DI: 00810022732571 · Model: 00810022732571 · INVIVOSCRIBE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LeukoStrat
Primary DI
00810022732571
Version / Model
00810022732571
Catalog Number
K4120361
Company Name
INVIVOSCRIBE, INC.
Labeler DUNS
836976779
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-30
Public Version
1
Public Version Date
2023-06-07
Public Version Status
New
Public Device Record Key
b3e2403b-7a59-40cf-a459-48ed2ae58ea5

Device Description

The LeukoStrat CDx FLT3 Mutation Assay is a PCR-based in vitro diagnostic test designed to detect internal tandem duplication (ITD) and tyrosine kinase domain (TKD) mutations D835 and I836 in the FLT3 gene in genomic DNA extracted from mononuclear cells obtained from peripheral blood or bone marrow aspirates of patients diagnosed with acute myelogenous leukemia (AML).

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OWD Somatic Gene Mutation Detection System

GMDN Terms

Code Name
60077 Acute myeloid leukaemia (AML) genetic mutation IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Primary 00810022732571

Premarket Submissions

Submission Number Supplement Number
P160040 006