RAMP® Infectious Disease Assays, Response Biomedical

About this item

The RAMP® Platform delivers superior sensitivity in the detection of Respiratory Syncytial Virus (RSV) by delivering objective, rapid test results in approximately 15 minutes. Results aid Physicians in making quick clinical decisions and therefore, provide efficient and effective treatment to patients. Rapid detection of RSV, combined with other infection control measures, may help healthcare facilities improve patient care and help protect at-risk populations.

Positive/Negative Quality Control swabs available
Approx. 15 minutes per test
Rapid aid in diagnosis
Nasal wash/aspirate, nasopharyngeal aspirate or nasopharyngeal swab samples acceptable
Standardized test procedure for all infectious disease assays
Qualitative test

The RAMP® RSV test is a qualitative, immunochromatographic test used for the detection of Respiratory Syncytial Virus (RSV) F-protein antigens in nasal wash, nasopharyngeal aspirate and nasopharyngeal swab samples. It is an in vitro diagnostic test that aids in the rapid diagnosis of RSV infections in symptomatic patients 21 years of age and younger.

Positive/Negative controlswabs are available for RAMP RSV tests.

It is an in vitro diagnostic test that aids in the rapid differential diagnosis of influenza viral infections in symptomatic patients.

Certifications: FDA Cleared. Health Canada Approved. CE Marked. ISO 9001 and ISO 13485 Certified.

Ordering information: The RAMP RSV assay can only be run on the RAMP 200 platform

Delivery: RAMP Infectious Disease test kits and Control Swabs should be stored at 15-30 °C (59-86 °F). Do not freeze.

Restricted Products: To process your orders without delay, please provide the required business documentation to purchase this product.

To order chemicals, medical devices, or other restricted products please provide ID that includes your business name & shipping address via email [email protected] or fax 484.881.5997 referencing your VWR account number. Acceptable forms of ID are:

• State issued document with your organization's Federal Tax ID Number
• State issued document with your organization's Resale Tax ID Number
• City or County issued Business License
• State Department of Health Services License
• Any other ID issued by the State that includes the business name & address

* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. Avantor will not lift restrictions for residential shipping addresses.

Specifications

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