FDA UDI In Commercial Distribution 🇺🇸 United States

Toxoplasma gondii IgM

DI: 00845533002110 · Model: FA8001M · ZEUS SCIENTIFIC, INC.
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Toxoplasma gondii IgM
Primary DI
00845533002110
Version / Model
FA8001M
Catalog Number
FA8001M
Company Name
ZEUS SCIENTIFIC, INC.
Labeler DUNS
080953946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-11
Public Version
1
Public Version Date
2025-11-19
Public Version Status
New
Public Device Record Key
934763c5-8f3e-4881-945a-54b5fc53d7d1

Device Description

The Toxoplasma gondii IgM is an indirect fluorescent antibody assay designed for the presumptive qualitative detection of IgM antibodies to T. gondii in human serum and for the presumptive diagnosis of acute, recent, or reactive T. gondii infection. To adquately assess the patient’s serological status; testing must be performed in conjunction with an anti-T. gondii IgG antibody assay. This product is not FDA cleared (approved) for use in testing (i.e., screening) blood or plasma donors. Performance characteristics have not been established for screening sera from 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
52441 Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay

Identifiers

Type ID
Primary 00845533002110

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius