ELISA HSV gG-1 IgG Smart Kit Test System SM9Z9761G

GUDID 00845533000673

The ZEUS ELISA HSV gG-1 IgG Test System is intended for the qualitative detection of type specific IgG class antibodies to Herpes Simplex Virus Type 1 (HSV-1) in human serum. The test is intended for testing sexually active individuals or pregnant women for aiding in the presumptive diagnosis of HSV-1 infection. The predictive value of positive or negative results depends on the population’s prevalence and the pretest likelihood of HSV-1. The test is not intended for donor screening or for self testing. The performance of this test has not been established for use in a pediatric population, neonates, children, or immuno-compromised patients.

ZEUS SCIENTIFIC, INC.

Herpes simplex virus 1 (HSV1) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Primary Device ID00845533000673
NIH Device Record Keydf8190d2-0d4a-404d-930a-40e294e8f96e
Commercial Distribution StatusIn Commercial Distribution
Brand NameELISA HSV gG-1 IgG Smart Kit Test System
Version Model NumberSM9Z9761G
Catalog NumberSM9Z9761G
Company DUNS080953946
Company NameZEUS SCIENTIFIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100845533000673 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-24

Devices Manufactured by ZEUS SCIENTIFIC, INC.

00845533002561 - RF IgM 2025-12-29 The Rheumatoid Factor (RF) IgM Test System is intended for the qualitative and semi-quantitative detection of RF IgM class antib
00845533002578 - RF IgM 2025-12-29 The Rheumatoid Factor (RF) IgM Test System is intended for the qualitative and semi-quantitative detection of RF IgM class antib
00845533002585 - Anti-M. pneumoniae IgG 2025-12-29 The Anti-M. pneumoniae IgG provides a means for the qualitative detection of IgG antibodies to Mycoplasma pneumoniae in human se
00845533002592 - Anti-M. pneumoniae IgG2025-12-29 The Anti-M. pneumoniae IgG provides a means for the qualitative detection of IgG antibodies to Mycoplasma pneumoniae in human se
00845533002608 - Anti-B. burgdorferi IgG 2025-12-29 The Anti-B. burgdorferi IgG is an enzyme-linked immunosorbent assay (ELISA) for the qualitative presumptive detection of IgG ant
00845533002615 - Anti-B. burgdorferi IgG 2025-12-29 The Anti-B. burgdorferi IgG is an enzyme-linked immunosorbent assay (ELISA) for the qualitative presumptive detection of IgG ant
00845533002622 - Anti-B. burgdorferi IgM2025-12-29 The Anti-B. burgdorferi IgM is an enzyme-linked immunosorbent assay (ELISA) for the qualitative presumptive detection of IgM ant
00845533002639 - Anti-Hama IgG 2025-12-29 The Anti-Hama IgG is a direct enzyme-linked immunosorbent assay for the detection and semi-quantitation of human antibodies to m

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.