This is an Applied Biosystems® 7500 Fast Dx Real-Time PCR Instrument with SDS v1.4 Software. It is a 96-well, 5-color real-time PCR instrument available for in vitro diagnostic use. The 7500 Fast Dx Real-Time PCR Instrument delivers the performance required for high-quality results in a 96- well format.

• 96-well format eases plate setup if automation is not available
• Accommodates tube strips, which can be capped immediately after pipetting each sample
• Fast mode completes runs in less than forty minutes
• Optional standard mode facilitates use of standard length real-time PCR assays without changing thermal cycling parameters
• 5-color variable excitation enables multiplex assays

Convenient 96-well Format
Compared to non 96-well formats, the 7500 Fast Dx Real-Time PCR Instrument minimizes the effort required to perform sample setup and allows the use of tube strips.

Intuitive Software to Run Pre-Optimized Protocols
The 7500 Fast Dx Instrument’s Sequence Detection Software v1.4 Security, Auditing, and E-Signature module offers the flexibility to develop assays and also run pre-optimized protocols for users operating in a secure environment.

Instrument Service and Support
The 7500 Fast Dx Real-Time PCR Instrument is supported by our AB Assurance Service Plan for Diagnostics, which includes:
• Instrument Installation Qualification, Operation Qualification, and Performance Qualification (IQ⁄OQ⁄PQ)
• Spectral calibration and software setup
• Emergency repair including parts and labor, and OQ⁄PQ after any major part change
• Planned maintenance every 12 months

In Europe: For in vitro Diagnostic Use. The 7500 Fast Dx Real-Time PCR Instrument meets the requirements of the in vitro Diagnostic Medical Devices Directive (98⁄79⁄EC). The CE IVD-registered 7500 Fast Dx Real-Time PCR Instrument is for distribution and use in specific European countries only.

In the United States of America: For in vitro Diagnostic Use. The 510 (k)-cleared (K082562) 7500 Fast Dx Real-Time PCR Instrument is for use with the CDC flu assay. The customer is responsible for any validation of assays, and compliance with any regulatory requirements that pertain to their procedures and instrument use.