JSD Domino INK refers to a line of compatible or alternative ink cartridges and fluids designed for use with Domino brand continuous inkjet (CIJ) printers. It's important to note that JSD is a different company (specifically, JASKAN SD TECHNOLOGIES INDIA PVT LTD) that manufactures these consumables, which are intended to be a lower-cost alternative to the original equipment manufacturer (OEM) inks produced by Domino.
Here are some key characteristics of JSD Domino INK based on available product descriptions:
Compatibility: The inks are specifically formulated to work with various models of Domino printers, including those in the G-Series and I-Tech series.
Ink Technology: JSD inks for Domino printers are typically Continuous Inkjet (CIJ) technology inks. They are also available in different types, such as solvent-based inks.
Capacity: The ink cartridges come in various sizes, commonly including 825 ml, 1000 ml, and 5-liter containers.
Colors: While black ink is the most common, other colors may be available.
Purpose: These inks are used for printing on various products and packaging in industrial settings for tasks like batch coding, date marking, and product identification.
Manufacturer: JSD Domino INK is manufactured by JASKAN SD TECHNOLOGIES INDIA PVT LTD, an Indian company.
Based on the search results, here is a description of the JSD Hitachi Ink Cartridge 1000ml:
The JSD Hitachi Ink Cartridge 1000ml is a compatible or alternative ink cartridge designed for use with Hitachi continuous inkjet (CIJ) printers. It is manufactured by Jaskan SD Technologies India Pvt Ltd, a company that specializes in producing compatible industrial inkjet inks.
Key Features and Specifications:
Capacity: 1000 ml (1 liter)
Ink Type: Continuous Inkjet (CIJ) ink, often solvent-based. There are different models, such as the JSD-0102, which may have specific ink types like "RX CIJ ink."
Color: The most commonly listed color is black.
Compatibility: It is designed to be a replacement for original Hitachi printer inks, compatible with various Hitachi inkjet printer models (e.g., UX Series, RX Series).
Purpose: The ink is intended for industrial applications, such as batch coding and marking on various surfaces.
Product Details:
Form Cassette
Brand Abbott
Country of Origin Made in India
To perform a test with i-STAT single-use cartridges, 2 to 3 drops of blood are applied to a cartridge, which is then inserted into an i-STAT 1 or i-STAT Alinity blood analyser. Results are available in approximately 2 minutes for most tests. The i-STAT System allows clinicians to stay with the patient to perform diagnostic testing to help accelerate clinical decisions and time to treatment.
This company is the one of the leading manufacturers and exporters of silica quartz in lumps, grits and powder. These products are used as a basic raw material for semicoductor, fiber optic, glass, artificial marble and granite, epoxy, paint, refractory and ceramic industries.
Product Details:
Operation Mode Fully Automatic
Number Of Chambers 2
Sample Mode Whole Blood, Capillary
Test Time 20 Min
Power AC or Battery
Cat. No 260300003
S.No Pima CD4 Cartridge Code
1 Pima CD4 Cartridge (Qty 100) 260100100 (Worldwide)
2 Pima CD4 Cartridge (Qty 25) 260100025 (Worldwide)
The enumeration of absolute numbers of T-helper cells (commonly referred to as a CD4 count) has become an essential part of monitoring the course of immunosuppression caused by the Human Immunodeficiency Virus (HIV) and the initiation of Anti-Retroviral Therapy.
The Pima CD4 test gives you the ability to monitor patients while they are still in your care. Consisting of the Pima Analyser and Pima CD4 Cartridge, the Pimaâ?¢ CD4 test enables CD4 T-cell analysis at the point-of-care from a fingerstick or venous whole-blood sample in only 20 minutes, providing an effective and affordable tool in the management of HIV patients, specifically designed to serve the needs of the healthcare professional in the field, the laboratory or the office.
Cat. No : 601430050. Truenat COVID-19 Chip-based Real Time PCR Test is a semi quantitative detection of SARS CoV-2 RNA in human oropharyngeal and nasopharyngeal swab specimen and aids in detection and confirmation of SARS CoV-2 infection and diagnosis of COVID-19. The test detects the E and Orf1a genes of the virus.
Providing you the best range of Molbio Trueprep Auto Universal Cartridge Based Sample Prep Device, Molbio Trueprep AUTO Universal Cartridge Based Sample Prep Kit, Molbio Trueprep AUTO MTB Sample Pre Treatment Pack Kit, Molbio Trueprep AUTO Universal Sample Pre-treatment Pack and Molbio Trueprep AUTO Transport Medium for Swab Specimen Pack with effective & timely delivery.
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : human whole blood/serum/plasma
Specimen volume : 5 Microliter
stored at 4-30 C
Cat No : CFPC-51
Anti-CCP Plus
Supporting to distinguish and diagnose rheumatoid arthritis
This test helps to diagnose and provide appropriate treatment for chronic systemic autoimmune diseases and rheumatism by quantifying Anti-CCP in the blood.
INTENDED USE :
ichroma Anti-CCP is a fluorescence Immunoassay (FIA) for the qualitative or semi-quantitative determination of human IgG autoantibodies to cyclic citrullinated peptides (CCP) in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of rheumatoid arthritis (RA) in combination with other clinical and laboratory findings.
For in vitro diagnostic use only.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately.
PRINCIPLE :
A synthetic cyclic citrullinated peptide (CCP) is immobilized on a porous membrane. After a sample is added to the sample port, detection buffer, consisting of fluorescent conjugated polyclonal antibody to human IgG, is loaded to the buffer port. The more anti-CCP antibodies in sample forms the more the peptide antigen/anti-CCP antibodies complex and leads to stronger intensity of fluorescence signal on detector anti-human IgG, which is processed by instrument for ichroma tests to show anti-CCP level in sample.
MATERIALS SUPPLIED :
REF CFPC-51
Components of ichroma Anti-CCP Cartridge Box:
- Cartridges 25
- Sample collectors 25
- ID Chip 1
- Instruction For Use 1 Box containing Detection Buffer Tubes
Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human whole blood/serum/plasma
Specimen volume ; 150 microliter
stored at 4-30 DegreeC
Cat No : CFPC-23-1
PCT
Assessing initial risk of bacterial infection and fatal sepsis
Diagnosis of sepsis is routinely performed in intensive care units (ICU) of all hospitals. Early detection of sepsis is very important in determining appropriate treatment as it is known to improve patient survival through a various therapeutic strategy for sepsis. The ichroma & AFIAS PCT test helps detect bacterial sepsis and assess the risk of developing septic shock.
INTENDED USE :
ichroma PCT is a fluorescence Immunoassay (FIA) for the quantitative determination of Procalcitonin (PCT) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of bacterial infection and sepsis.
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.
The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PCT concentration in sample.
STORAGE AND STABILITY:
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately.
MATERIALS SUPPLIED :
REF CFPC-23
Components of ichromaâ?¢ PCT Cartridge Box:
- Cartridges 10
- ID Chip 1
- Instruction For Use 1 Box containing Detection Buffer tubes
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Specimen : human serum/plasma
Specimen volume : 50 Microliter
Cat. No. : CFPC-47
INTENDED USE :
ichromaâ?¢ Vitamin D is a fluorescence Immunoassay (FIA) for the quantitative determination of total 25(OH)D2/D3 level in human serum/plasma. It is useful as an aid in management and monitoring of regulating the concentration of calcium and phosphate in the bloodstream and promoting the healthy growth and remodeling of bone.For in vitro diagnostic use only.
PRINCIPLE :
The test uses a competitive immunodetection method. In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of 25(OH)D3 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. The releasing buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. Opened detection buffer and releasing buffer are stable for 12 months at 2-8 C if kept capped in original container and free from contaminations. After the cartridge pouch is opened, the test should be performed immediately.
MATERIALS SUPPLIED :
REF CFPC-47Components of ichroma Vitamin D Cartridge Box:- Cartridges 25- Sample Mixing Tubes 25- ID Chip 1- Instruction For Use 1 Detection Buffer Vial (3 mL) 1 Releasing Buffer Vial (2 mL) 1
Product Details:
Brand ; Boditech Med Incorporated
Size : 25 T
Samples: human whole blood/serum /plasma
Specimen volume human whole blood/serum/ plasma
stored at 4-30 C
Cat. No. : CFPC-66
Human Chorionic Gonadotropin (�²-hCG)
Distinguish pregnancy and abnormal pregnancy
The IhCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome.
INTENDED USE :
ichroma -HCG Plus is a fluorescence Immunoassay (FIA) for the
quantitative determination of -HCG in human whole blood/serum
/plasma. It is useful as an aid in management and monitoring of beta
human chorionic gonadotropin (hCG) level in human
For in vitro diagnostic use only.
PRINCIPLE :
The test uses a sandwich immunodetection method; Dried
antibodies in the detector tube, once diluted with the diluent, bind
with antigens in the sample to form antigen-antibody complexes.
These complexes then migrate through the nitrocellulose matrix and
are captured by another sets of immobilized antibodies on the test line.
The more antigens in the sample, the more antigen-antibody
complexes, which leads to a stronger fluorescence signal. This signal
then is interpreted by the reader to display the �²-HCG concentration in
the sample.
STORAGE AND STABILITY :
The cartridge is stable for 20 months (while sealed in the original
aluminum foil pouch) if stored at 4-30 C.
The detector, diluent and sample diluent are stable for 20 months
if stored at 2-8 C.
After the cartridge pouch is opened, the test should be
