Penguin Sucker / Nasal Aspirator

When a baby is stuffed up, the mucus from a baby's nose will affect their ability to breath, eat and sleep. Therefore, a infant aspirator is a baby must have item. The nasal aspirator for sale is compact and easy to carry. You can carry it whenever and wherever. And its detachable design is convenient for cleaning, while the anti-reflux design can prevent the mucus from back into the nose. Besides, this infant nasal aspirator uses high-quality motor to ensure low-voice, so that the baby can enjoy comfortable nasal cleaning experience in quiet environment.

Is nasal aspirator useful?
Nasal Aspirator
First
Nasal congestion in babies can be very stressful for babies, as babies may experience distress and feeding problems from a blocked nose. The impact on daily life can be disturbing, which can affect sleep patterns throughout the family.

Second
Thus nasal aspirator is a must-have device for every family prepared for their baby, which can help you safely and naturally clear out the unwanted fluid and mucous from babys nose.

Third
And its useful for you to use before the baby sleeps. It can help baby clearly breathe, easily feed and restful sleep.

Fourth
Besides, removing the excess fluid and mucus can help baby prevent further diseases, such as coughing, ear infections, and abdominal discomfort. After using, its easy for you to clean.

How does baby nasal aspirator work?

First
Nasal aspirator is an efficient, safe and gentle way to remove the unwanted fluid and mucus from babys nose for clearly breathing, better sleeping and eating.

Second
When the motor provides suction, the tip of the nose enters the child's nose.

Third
These machines usually have a variety of suction settings to suit children of different ages.

Fourth
Usually, we recommend that parents should keep babys body flat, letting her chin tilt up slightly and put a few drops of normal saline in babys each nostril to liquefy secretions, then use the nasal aspirator.

As a professional nasal aspirator supplier, JOYSTAR provides sterilizer and dryer, electric breast milk pump, breast feeding products, newborn nose cleaner, nasal suction, etc. For more, please feel free to contact us!

Intended Use

The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens.

Principle

The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.

Storage and Stability

1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch.

2.The test must remain in the sealed pouch until use.

SARS-CoV-2 (COVID-19) infection has been declared a pandemic by WHO. Among the 7 qPCR protocols released by WHO, we chose USA-CDC protocol; however, our scientists quickly realized the risk of false-negative detection due to dimer-dimer problems in this protocol. So, we developed an optimized kit that overcame this problem. Unlike many other companies, we produce every single component of its kit by itself, reducing the risk of mistakes during production. Our qPCR kits have over 99% accuracy. SARS-CoV-2 qPCR Detection Kit also has a fully synthetic and non-pathogenic positive control which eliminates the possibility of false-negative results due to enzymatic problems.

FOR COLLECTION AND TRANSPORT OF SAMPLESFOR NUCLEIC ACID AMPLIFICATION TESTS
Intended use:

VIROSWAB/TRANSFER is a transport system used for the collection and transport of cells from clinical samples or from the environment, for isolation of nucleic acids that will be used in nucleic acid amplification tests. Summary and explanation of the test: Amplification of nucleic acids isolated of the cells obtained from clinical samples or from the environment by methods like polymerase chain reaction (PCR) is widely used for various purposes like detection of infectious agents, identification of their genotypes, identification of DNA sequences that lead to genetic diseases, drug resistance, etc. The sensitivity of these methods is very much dependant on the appropriate collection and transport of the samples. VIROSWAP/TRANSFER is a kit prepared to enable this. VIROSWAP/TRANSFER is made up of two parts: Sterile dacron swab in a plastic package for collecting the sample and sterile transport medium in a crack-proof plastic tube. Samples obtained by the dacron swab is put in the transport medium. Specimens like a biopsy, scrapings, discharge can directly be put into the medium. Limitations: RNA molecules are very susceptible to nuclease digestion that may be coming from degrading cells. If amplification is intended to be done using RNA molecules as a template, it is recommended to transport the samples in an icebox and isolate nucleic acids within 4 hours.

Principles of the procedure:

VIROSWAB/TRANSFER is designed in a way to enable easy collection and appropriate transport of the samples. Polycarbonate tubes will not crack as glass tubes when the samples are frozen to preserve for an extended period of time. On the other hand the glass like transparent structure makes it easy to visualize and manipulate the samples. Dacron swab is kept dry; after collecting the sample the shaft of the swab is broken and the swab is placed into the tube containing the transport medium. The shaft of the swab is made from special plastic to enable easy breaking. The transport medium contains tris which keeps the pH around 8.0, which is suitable for nucleic acid preservation. Samples may contain nucleases (DNAse and RNAse) which will digest free nucleic acids and prevent their amplification. These enzymes require Mg++ as their co-factor to be functional. EDTA that is included in the transport medium strongly binds Mg++ and thus inhibits nucleases and preserve nucleic acids. Ingredients:

Sterile dacron swab in a plastic package.

Nucleic acid transport medium (20mM Tris (pH 8.0), 2mM EDTA) 3ml in plastic tube.

COVID-19 Ag Rapid Test Device

A RAPID TEST FOR THE QUALITATIVE DETECTION OF NOVEL CORONAVIRUS ANTIGENS IN NASAL SWAB AND NASAL ASPIRATE SPECIMENSS.

Relative sensitivity: 84.4%
Relative specificity: >99%
Overall agreement: 97.8%
Specimen: swab, 10-20 minutes to get results

1.100% silicone
2.Designed for nasal & gastric introduction for nutrition & aspiration of intestinal secretion.
3.Provided with full-length radio-opaque line for checking the tube placement.
4.Provision of four eye-holes for efficient aspiration.
5.Marked at 45, 55, 65, 75cm from the distal end.
6.Sterile, Non-toxic and Pyrogen free.

The COVID-19 RT-PCR Peptide Nucleic Acid (PNA) KIT is a real-time reverse transcription (RT)-Polymerase chain reaction (PCR) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in respiratory specimens such as nasopharyngeal swabs, oropharyngeal swabs, anterior nasal swabs, midturbinate nasal swabs, bronchoalveolar lavage (BAL), and nasopharyngeal wash/aspirates or nasal aspirates collected from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests.

Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities.

Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.

The COVID-19 RT-PCR PNA KIT is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR PNA KIT is only for use under the Food and Drug Administrations Emergency Use Authorization.