Datascope Accutorr Plus
Datascope · Model Accutorr Plus
Lightweight, portable design (weighs less than 5 lbs) for easy mobility in preoperative and postoperative areas. Non-invasive blood pressure, SpO2, and pulse rate measurement for comprehensive patient monitoring. Configurable technology allows adjustments for patient size, interval time, alarms, inflation pressure, audio levels, and more.\ Large, easy-to-read display with customizable controls for enhanced usability. Quick-connect, single hose fittings for convenient setup and use. Flexible databases for customizable settings and patient data management. IV pole or bed rail attachment for versatile mounting options. Battery operation ensures mobility and portability in various clinical settings. Stores up to 100 readings, instantly accessible for historical data review. Predictive thermometer module for enhanced temperature monitoring. Printer module for instant documentation and patient record generation. The Datascope Accutorr Plus is an ideal solution for biomedical engineers and healthcare providers seeking a reliable, portable, and easy-to-configure multi-parameter monitor that offers comprehensive patient care with minimal setup time.
Key tips
- ·A no-signal/flatline alarm gets checked on the patient first, not the monitor - rule out a real clinical event before troubleshooting.
- ·Recalibrate NIBP against a reference manometer, not just a self-test pass.
- ·Reused patient cables (SpO2, ECG leads) are a common source of intermittent-fault complaints - swap the cable before the module.
Typical Failure Modes
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
NIBP will not measure or is inaccurate
HighSymptoms: NIBP times out, cuff will not inflate / hold, readings implausible or fail against a reference.
Root cause: Internal NIBP pump or valve, a cuff / hose leak, or a pressure-transducer / calibration fault.
SpO2 no signal / inaccurate
MediumSymptoms: No saturation value or a poor pleth with a good site.
Root cause: Worn SpO2 sensor / cable, or the SpO2 module.
Temperature channel fault
MediumSymptoms: No or implausible temperature.
Root cause: Probe or cable fault.
Battery / power fault
MediumSymptoms: Short battery run time, will not power on or charge.
Root cause: Aged battery pack.
Printer / recorder fault
LowSymptoms: No or faint strip, paper jam.
Root cause: Thermal print head or paper handling.
Serviceable Parts & Consumables
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
Patient cable set (ECG / IBP / SpO2 / temp)
Class Frequent wear itemRel. cost $$R&R Easy
NIBP cuff and hose
Class Frequent wear itemRel. cost $R&R Easy
Internal NIBP pump / valve
Class Major service partRel. cost $$$R&R Difficult
SpO2 sensor / cable
Class Frequent wear itemRel. cost $$R&R Easy
Battery pack
Class Periodic replacementRel. cost $$R&R Fairly easy
Thermal print head / paper
Class Periodic replacementRel. cost $R&R Fairly easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Patient cable set (ECG / IBP / SpO2 / temp) | Frequent wear item | $$ | Easy |
| NIBP cuff and hose | Frequent wear item | $ | Easy |
| Internal NIBP pump / valve | Major service part | $$$ | Difficult |
| SpO2 sensor / cable | Frequent wear item | $$ | Easy |
| Battery pack | Periodic replacement | $$ | Fairly easy |
| Thermal print head / paper | Periodic replacement | $ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
- ·Routine cable and lead-wire inspection for fraying/wear
- ·Battery conditioning cycle
- ·NIBP calibration check against a reference manometer
- ·ECG / SpO2 accuracy verification against a patient simulator
- ·Annual electrical safety test
Error Codes
Extracted directly from this unit's own service manual.
8810Retry - Unable to Measure Motion artifact, cycle time-out, weak pulsations or no pulsations. A triple beep tone is generated.
8811Retry - Pump Higher Insufficient cuff pressure. A triple beep tone is generated.
8812Stop - Cuff Overpressure Excessive cuff pressure detected by the software. A triple beep tone is generated.
8813Stop - Unable to Measure 4 successive measurement attempts failed. A triple beep tone is generated.
8830Check Probe Tissue contact may have been lost.
8831Replace Probe Defective probe or connection.
8850No Sensor No sensor connected.
8851Sensor Off Sensor not on patient. (Masimo® SpO2 only)
8852Interference Interference on signal. (Masimo® SpO2 only)
8853Pulse Search Unit cannot find signal. (Nellcor® SpO2 module will report "Pulse Search"-8853- when the sensor is not on the patient.)
8854Weak Pulse Weak pulse detected. (Masimo® SpO2 only)
8856Check Sensor Sensor problem. (Masimo® SpO2 only)
8857PR<21 Pulse rate is less than 21 bpm. (Nellcor® SpO2 only)
8858PR>249 Pulse rate is greater than 249 bpm. (Nellcor® SpO2 only)
984*NIBP Hardware Failure NIBP A/D failure detected.
985*NIBP Overpressure Circuit not Programmed The overpressure circuit is not set to the current patient size.
986*NIBP Overpressure Circuit not Tracking The two pressure transducers are not tracking each other.
987*Stop - Hardware Overpressure Excessive cuff pressure detected by hardware overpressure sensor. A triple beep tone is generated.
988*TEMP Bad Calibration Thermometer needs calibration.
990*TEMP Illegal Mode Thermometer switch is set wrong.
991*TEMP Module Failed Thermometer internal failure.
995*SpO2 Uncalibrated SpO2 fails calibration check.
996*SpO2 Failure SpO2 failed self-test.
Troubleshooting Approach
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Symptom: NIBP problem
- Leak-test the cuff and hose.
- Run the monitor's NIBP calibration verification.
- Check for a kinked hose or a positional patient limb.
- Verify NIBP against a reference / simulator.
- Refer the monitor for internal pump / valve service if it persists.
Symptom: SpO2 no signal
- Fit a fresh SpO2 sensor and check the site.
- Swap the SpO2 cable.
- Confirm the pleth and signal-quality indicator.
- Replace the SpO2 module if a good sensor and cable do not fix it.
- Verify against a simulator.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- ICU / CCU
- Emergency Department
- OR / PACU
- General med-surg floors
- Step-down units
- Telemetry units
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
During IAB catheter insertion, the introducer dilator may fracture at the hub, leaving the body of the introducer dilator housed within the sheath. Risks to health include damage to the femoral artery, descending aorta, or embolization; surgical intervention and delay of IAB therapy may also result. Firm has received 10 complaints, including 3 serious adverse events and 1 patient death.
- RECALL
Certain lots containing undersized dilator.
- RECALL
The device was distributed with the outer carton labeled with the manufacture date and the expiry date reversed. This showed the product as expired before it was manufactured.
- RECALL
Maquet/Getinge is initiating a voluntary product removal involving four lot numbers of SENSATION PLUS 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK since during internal pressure (leak) testing of the SENSATION PLUS 8Fr. 50cc, IABC, failures related to the tip seal leak were identified.
- RECALL
The Anestar and Anestar Plus Anesthesia System may produce periods of high Positive End-Expiratory Pressure (PEEP), in both manual and mechanical ventilation mode due to an issue with the Applied Pressure Limit (APL) valve.
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