SEARCH RESULTS FOR: 男M♥飞机号@zykaifa中国云南省普洱市墨江哈尼族自治县(41984 results)
Only the first 10,000 results were returned. Filter these results or refine your query. Some pre-built queries with more than 10,000 results are available for download.
Anti-HBc IgM CVM - IMMULITE - CONS
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
10373676
In Commercial Distribution
- 00630414978017 ()
L2MCCVM
- Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, control
The ImmunoFA Toxo IgM Test is an immunofluorescence test for the presumptive detection and titration of IgM antibodies to Toxoplasma gondii in human serum and is presumptive for the diagnosis of acute, recent, or reactivated T. gondii infection. It is intended that the ImmunoFA Toxo IgG Test be performed in conjunction with this assay. This product is not FDA cleared (approved) for use in testing (i.e., screening) blood or plasma donors.
Genbio
800-1300
In Commercial Distribution
- 00613745013008 ()
- 100 tests
1300
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
T. pallidum WB IgG Positive Control, 250µl
MARDX DIAGNOSTICS, INC.
40-5023
In Commercial Distribution
- 05391516749138 ()
40-5023
- Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control
T. pallidum WB Negative Control, 250µl
MARDX DIAGNOSTICS, INC.
40-5021
In Commercial Distribution
- 05391516749121 ()
40-5021
- Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control
The ZEUS IFA Toxoplasma gondii IgM Test System 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.
ZEUS SCIENTIFIC, INC.
FA8001M
In Commercial Distribution
- 00845533001526 ()
FA8001M
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
PK7400 TP HA CONTROLS is intended for use with the PK7400 TP HA REAGENT (B11186) for the qualitative screening of blood and plasma donors for the detection of Treponema pallidum IgG and IgM antibodies in human serum, EDTA plasma and CPDA plasma using the Beckman Coulter PK7400 Automated Microplate System.
NEWMARKET BIOMEDICAL LIMITED
B11187
In Commercial Distribution
- 05060515140047 ()
- 16 x 5mL
- Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control
Respiratory Panel Cartridge
GENMARK DIAGNOSTICS, INC.
ePlex Respiratory Panel (RP)
In Commercial Distribution
- 00857167005016 ()
KT022287
- Hepatitis G virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
No Description
Roche Diagnostics GmbH
04618858190
In Commercial Distribution
- 04015630921485 ()
04618858190
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay
No Description
Roche Diagnostics GmbH
11876333160
Not in Commercial Distribution
- 04015630911622 ()
11876333160
- Hepatitis B virus core immunoglobulin M (IgM) antibody IVD, control
No Description
Roche Diagnostics GmbH
07028024190
In Commercial Distribution
- 04015630940318 ()
07028024190
- Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay