Smiths Medical BCI FingerPrint
Smiths Medical · Model BCI FingerPrint
Integrated printer provides immediate hard-copy documentation of Desaturation Summary Report. Easy-to-use, 2-key operation. 3-mode versatility: spot checking, data collection, and data transfer. Display disappears during data collection, conserving power and reducing patient distractions. Download an entire 8-hour study to a PC using commercially available software in a matter of minutes. View desaturation and heart rate data via optional PC data management software. Economically download and print 2 full overnight sleep screens on one set of 4 “AA” alkaline batteries. Genuine BCI® reusable and disposable sensors available.
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
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
ECG lead-off / artifact
MediumSymptoms: Flat or noisy ECG, frequent lead-off alarms.
Root cause: Worn electrodes, loose leads, or dry gel.
NIBP measurement error
MediumSymptoms: Cuff fails to inflate, erroneous BP, long cycle.
Root cause: Pump/valve wear or cuff leak.
Internal battery depletion
HighSymptoms: Short backup time, battery alarm on transport.
Root cause: Aged backup battery.
Display / touch panel fault
LowSymptoms: Dim, flickering, or unresponsive screen.
Root cause: Backlight or digitizer failure.
Serviceable Parts & Consumables
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
ECG patient cable & lead set
High-turnover; keep inventory.
Class Frequent wear itemRel. cost $$R&R Easy
SpO2 sensor (adult/ped/neo)
Class Frequent wear itemRel. cost $$R&R Easy
NIBP cuff & hose
Consumable per patient.
Class Periodic replacementRel. cost $R&R Easy
Rechargeable backup battery
Class Periodic replacementRel. cost $$R&R Fairly easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| ECG patient cable & lead set High-turnover; keep inventory. | Frequent wear item | $$ | Easy |
| SpO2 sensor (adult/ped/neo) | Frequent wear item | $$ | Easy |
| NIBP cuff & hose Consumable per patient. | Periodic replacement | $ | Easy |
| Rechargeable backup battery | Periodic replacement | $$ | 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
Troubleshooting Approach
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: ECG lead-off / artifact
- Confirm the presentation - typically flat or noisy ECG, frequent lead-off alarms - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: worn electrodes, loose leads, or dry gel.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the eCG patient cable & lead set per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: SpO2 probe / sensor failure
- Confirm the presentation - typically no pleth, SpO2 drops to --- or false low - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: lED/photodiode aging or cable damage.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the spO2 sensor (adult/ped/neo) per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Technical Specs
- Height
- 6.6 in
- Length
- 1.43 in
- Pulse Rate Range
- 30-254 BPM
- Weight
- 13 oz
- Operating Life
- 24 sec no printing
- SpO2 Range
- 0-100%
- Width
- 2.75 in
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
Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway circuit could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.
- RECALL
Some printing modes on the devices may not function properly (tabular data printing, real-time continuous printouts, and automatic interrupt print feature).
- RECALL
The Auxiliary Serial Input/ Output Modes on the Advisor do not function as expected, resulting in data formatting issues or incorrect data being transmitted in or out of the serial port into a data collection system.
- RECALL
In rare instances, the BCI Remote Alarm Cables (BCI Cable) are not transferring alarms when used with some remote nurse alarm systems.
- RECALL
Recent improvements were made to the Advisor case plastic resulting in the inserts being deeply embedded into the plastic. This affects the ability of the monitor to be adequately secured on the wall mount bracket or roll stand bracket, resulting in the monitor falling off. There have been no adverse events or injuries reported.
- RECALL
Due to a component that may be installed backwards, the device may turn off or may immediately reset.
- RECALL
The Smith Medical PM, Inc. BCI 3180 Pulse Oximeter tantalum capacitors C38, C72, C74, and C98 were installed backwards during assembly at the board manufacturer. This exposes the components to reverse polarity voltages that may lead to their pre-mature failure. As a result, the identified monitors may exhibit failure modes such as the monitor may shut down and not produce alarms or signals to
- RECALL
Turn off unexpectedly/ Not turn on : monitors turned off unexpectedly sounding the critical failure alarm. Advisor Vital Signs monitors that were off, would not turn back on.
Troubleshoot this device with Bio
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →