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IFA AAS Mouse Kidney/Stomach/Liver Test System

FDA UDI

by Zeus Scientific, Inc.

Identity

Trade Name
IFA AAS Mouse Kidney/Stomach/Liver Test System FDA UDI
Generic Name
Multiple systemic lupus erythematosus (SLE)-associated antibody IVD, kit, fluorescent immunoassay FDA UDI
Device Name
The ZEUS IFA Autoantibody Screen (AAS) Mouse Kidney/Stomach/Liver Tissue Test System is designed for the qualitative and semi-quantitative detection of antinuclear, mitochondrial, smooth muscle and parietal cell antibodies by the indirect fluorescent antibody IFA technique. It aids in determining SLE and differentiating clinically similar connective tissue disorders, and is for In Vitro diagnostic use. FDA UDI
Model / Reference
FA3403 FDA UDI
Description
The ZEUS IFA Autoantibody Screen (AAS) Mouse Kidney/Stomach/Liver Tissue Test System is designed for the qualitative and semi-quantitative detection of antinuclear, mitochondrial, smooth muscle and parietal cell antibodies by the indirect fluorescent antibody IFA technique. It aids in determining SLE and differentiating clinically similar connective tissue disorders, and is for In Vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
FA3403 FDA UDI
Primary DI / UDI-DI
00845533001441 FDA UDI
GMDN Term
Multiple systemic lupus erythematosus (SLE)-associated antibody IVD, kit, fluorescent immunoassay FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple systemic lupus erythematosus (SLE)-associated antibody IVD, kit, fluorescent immunoassay

IFA AAS Mouse Kidney/Stomach/Liver Test System by Zeus Scientific, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple systemic lupus erythematosus (SLE)-associated antibody IVD, kit, fluorescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dba1f48b-a257-4d31-88df-a4039dc59b75 35 fields · synced May 30, 2026