FDA UDI In Commercial Distribution 🇺🇸 United States

ELISA T. gondii IgM Test System

DI: 00845533001229 · Model: 8Z8651M · ZEUS SCIENTIFIC, INC.
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELISA T. gondii IgM Test System
Primary DI
00845533001229
Version / Model
8Z8651M
Catalog Number
8Z8651M
Company Name
ZEUS SCIENTIFIC, INC.
Labeler DUNS
080953946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
27cb52f4-2ec9-4000-b12e-e92f9850d0c8

Device Description

The ZEUS ELISA Toxoplasma gondii IgM Test System is an enzyme-linked immunosorbent assay designed for the presumptive qualitative detection of IgM antibodies to Toxoplasmaplasma gondii in human serum and for the presumptive diagnosis of acute, recent, or reactive Toxoplasma gondii infection. To adequately assess the patient’s serological status, testing must be performed in conjunction with an anti-Toxoplasma gondii IgG antibody assay. This product is not FDA cleared (approved) for use in screening blood or plasma donors. This assay’s performance has not been established for screening of prenatal women or newborns.

Device Characteristics

Single Use
Yes
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
No
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

GMDN Terms

Code Name
52440 Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 00845533001229

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius