The RAPIDPoint 500e System elevates Siemens Healthineers blood gas offering to a new level, allowing you to spend more time focused on patient care. Implement a proven end-to-end blood gas solution that reduces the daily burden of device management and enables you to give your full care and attention where it matters most.
With an improved user experience, the analyzer transforms care delivery, setting an elevated standard in simplicity, quality assurance, and data security for healthcare organizations
Parameters |
Analyte |
Blood Gas |
pH, pCO2 and pO2 |
Electrolytes |
Na+, K+, Ca++ and CI– |
Metabolites |
Glucose and Lactate |
CO-oximetry |
tHb, sO2, O2Hb, HHb, COHb, MetHb and Neonatal Total Bilirubin |
The RAPIDPoint 500e system also supports additional sample types: pleural fluid pH; Na+, K+, Ca++, Cl–, pH, pCO2, and HCO–3(act)† for dialysate fluid‡ samples.
†pH, pCO2, and HCO–3(act) are provided for reference only.
Sample volume |
100 µL |
Analysis |
Time to results is approximately 60 seconds |
Quality Control |
Automatic QC or ampule QC
Three levels of independent quality control solutions Customizable QC schedule |
Measurement Cartridge |
Cartridge initialization time is approximately 24 minutes |
Use life |
28 days onboard, or maximum number of tests
|
Integrated Barcode Scanner |
1D barcode symbologies – Code 128, Codabar, Code 39, Character/Digit, Interleaved 2 of 5 2D barcode symbologies – PDF417, MicroPDF417, Datamatrix, QR Code, Micro QR Code, Aztec, and Maxicode |
Operating System |
MICROSOFT WINDOWS 10 IoT
|
Communications | LIS Wireless Dual-port transmission via Ethernet and serial port POCcelerator™ Data Management System POCcelerator SE Data Management System |
Healthcare professionals are increasingly under pressure to deliver quality care in busy critical care settings. Any delay, distraction, or concern in the generation and reporting of test results physicians rely on can add to the operational burden and take time and focus away from the patient.
To give you confidence in every result while reducing the time to diagnosis and treatment, the RAPIDPoint 500e system provides robust accuracy from sample to sample by leveraging the Siemens Healthineers-designed Integri-sense™ Technology—the guardian of patient results. Integri-sense Technology is a comprehensive series of analyzer functional checks and flagging mechanisms designed to deliver accurate test results. It performs frequent quality and blood integrity checks before, during, and after every patient sample. Three levels of independent automatic quality control, multiple calibration routines, and advanced software algorithms combine to enable the RAPIDPoint 500e analyzer to be ready to generate reliable and clinically actionable test results each and every time.
Depend on the RAPIDPoint 500e system to raise the bar in blood gas IT security at your facility with the latest defenses to guard confidential patient data coupled with the leading built-in technology to protect your institution from external cybersecurity threats. The WINDOWS 10 operating system has been equipped with McAfee embedded anti-malware, which blocks unknown and unauthorized programs from running. Other key security advantages include a two-step authentication process, an encrypted password requirement for patient data transfer, and the inclusion of a firewall to block hacking attempts.
This user-friendly and maintenance-free analyzer provides the patient results most needed by clinicians in critical care environments. The simplicity of the RAPIDPoint 500e system centers on the fact that it is a fully cartridge-based analyzer, with no maintenance required. The measurement cartridge includes the planar sensors, sample probe, and CO-ox chamber, so all these components are replaced with every new cartridge.
One of the unique features of the RAPIDPoint 500e system is the sample port. Syringe and capillary samples are handled in exactly the same way, and operator variability is eliminated with hands-free automatic sampling. Only 100 µL of sample is aspirated, and the sample port is part of the advanced clot management and air bubble detection mechanism.
Integri-sense Technology is the guardian of patient results. The system performs frequent quality and sample integrity checks before, during, and after every patient sample. Automatic quality control, comprehensive calibrations, and advanced software algorithms combine to enable the analyzer to be ready to generate reliable, clinically actionable results each and every time, delivering confidence with every result.
Service is essential to keep medical equipment operational and safe. Our Nordic service team consists of experienced service technicians stationed across the Nordic countries. Our service technicians are ready to take on your every service need.”
Nasal PAP ventilation system
The SuperNO2VA nasal PAP ventilation system uses the flow from any oxygen source. Delivers positive airway pressure to stent open the upper airway, allowing for the preoperative delivery of positive pressure ventilation and oxygen for patients with a decreased level of consciousness. The SuperNO2VA™ nasal PAP ventilation device is available in medium and large sizes and is offered as a standalone mask with a head strap and as a system, kitted with a hyperinflation bag. These configurations offer flexibility as it allows the SuperNO2VA™ nasal PAP ventilation device to be used with either an anesthesia machine or with only an oxygen flow meter.
The dual-valved LiteAire MDI holding chamber: Collapsible, disposable paperboard design.
The LiteAire® collapsible MDI holding chamber is a unique MDI holding chamber and an innovative alternative. LiteAire’s unique dual-valved MDI holding chamber design delivers pop-up convenience and effective drug output at a fraction of the cost of most plastic holding chambers. In many clinical settings, the LiteAire can reduce costs by replacing existing rigid plastic holding chambers or inefficient spacers with a paperboard alternative. The unique design allows the LiteAire to be reused by a patient over multiple doses and meets and often exceeds the performance of plastic holding chambers.
Gentle respiratory support to neonates worldwide
For over two decades, the Infant Flow™ nCPAP system has delivered gentle respiratory support to thousands of neonates worldwide. The system, combined with the patented variable flow generator, provides NPPV by offering nasal CPAP and Biphasic modalities. The system takes the work out of breathing, freeing precious calories to be used for growth and development.
Innovative phototherapy cover made of a high-tex material
BiliCap® is made of a 3-layered functional specialty knit fabric. A highly elastic, breathable membrane in the core assures the phototherapy cover’s imperviousness to light. The 3D knit spacing fabric underneath ensures optimum noise attenuation, provides an anti-slip effect and permanently retains the cover’s shape.
Additionally, the material is characterised by low weight and contains an active substance with permanently antimicrobial effect.
BiliCap® optimally shields the surrounding treatment places against the high light intensity while providing fast and flexible access via 4 side and 2 head/foot flaps. The one-size design allows flexible use, fitting all incubator models commonly available on the market. BiliCap® is certified according to Oeko-Tex® Standard 100, washable up to 95 °C and suitable for tumble-drying. Guaranteed permanence of function and colour even in the case of frequent laundering. Available in 2 colours with individual ornaments and embroidery.
Timik ApS
Sivlandvænget 27B, st. th.
5260 Odense S
Tel: +45 8230 6700
Org.nr 36089210