FDA.reportPublic FDA data

Kalazar Detect Rapid Test for Visceral Leishmaniasis

Primary DI
B379INS0251
Brand
Kalazar Detect Rapid Test for Visceral Leishmaniasis
Company
INBIOS INTERNATIONAL, INC
Model
INS025
Catalog number
INS025
Published
2018-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
LOOReagent, Leishmanii Serological

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LOOReagent, Leishmanii SerologicalMicrobiology1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B379INS0251PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Leishmania donovani immunoglobulin G (IgG) antibody IVD, kit, immunochromatographic test (ICT), rapidA collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin G (IgG) antibodies to the parasitic protozoan Leishmania donovani in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method. This test is commonly used in the laboratory or in point-of-care analyses.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
004006628
Device count
1
Kit
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B379COVGRE1SCoV-2 Detect™ IgG Rapid TestCOVG-RE2022-12-08
B379RCFP251COVID/Flu A&B RespiraDXTM Rapid TestRCFP-25RCFP-252025-10-06
B379RCFPCK101COVID/Flu A&B RespiraDX Rapid Test Control Kit Box (10 sets)RCFP-CK102025-10-06
B379RCFPCK21COVID/Flu A&B RespiraDX Rapid Test Control Kit Box (1 set)RCFP-CK22025-10-06
B379RCFS21COVID/Flu A&B RespiraDXTM Rapid Self-TestRCFS-2RCFS-22025-10-06
B379RCFS41COVID/Flu A&B RespiraDXTM Rapid Self-TestRCFS-4RCFS-42025-10-06
B379COV2E0Smart DetectTM SARS-CoV-2 rRT-PCR KitCOV2-E2020-07-15
B379COVAF201SCoV-2 Ag Detect™ Rapid TestCOVAF-202024-09-13
B379COVAF501SCoV-2 Ag Detect™ Rapid TestCOVAF-502024-09-13
B379STNG11Strongy DetectTM IgG ELISASTNG-12024-09-13
B379ZKM21ZIKV Detect™ 2.0 IgM Capture ELISAIVD2019-05-24
B379COVNE1SCoV-2 Detect™ Neutralizing Ab ELISACOVN-E2022-12-08
B379C19S21COVID-19 Detect™ Rapid Self -TestC19S-22026-01-16
B379RCFPCK201COVID/Flu A&B RespiraDX Rapid Test Control Kit Box (20 sets)RCFP-CK202025-10-06
B379AAP11Active Anthrax Detect Plus Rapid TestAAP-12023-03-03
B379CAGS21SCoV-2 Ag Detect™ Rapid Self-TestCAGS-22022-12-08
B379COVAGRC1SCoV-2 Ag Detect™ Rapid TestCOVAG-RC2022-12-08
B379COVEG1SCoV-2 Detect™ IgG ELISACOVE-G2022-12-08
B379COVEM1SCoV-2 Detect™ IgM ELISACOVE-M2022-12-08
B379CL0251CL Detect Rapid Test for Cutaneous LeishmaniasisCL025CL0252018-09-24

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
05391516747943Trinity BiotechMARDX DIAGNOSTICS, INC.LOO2016-09-19
05391516747585Trinity BiotechMARDX DIAGNOSTICS, INC.LOO2016-09-18
05391516748698Trinity BiotechMARDX DIAGNOSTICS, INC.LOO2016-09-18
05391516748919Trinity BiotechMARDX DIAGNOSTICS, INC.LOO2016-09-18
05391516748926Trinity BiotechMARDX DIAGNOSTICS, INC.LOO2016-09-18