KOPP Development Inc. · Model FerrAlert™ HALO PRESCREEN
• Instantly PINPOINTS location of the ferromagnetic object, allowing Technologist to quickly identify and remove the ferromagnetic threat – NO invasive PAT-DOWN required • Limits alarm fatigue – Patented technology suppresses irrelevant warnings and false positive alarms caused by hallway traffic • 24 location-accurate sensors for uniform sensitivity, reliability and usability • An intelligent pre-alarm indicator - Constantly monitors the ambient magnetic field and provides early visual warning of approaching ferrous objects • No-Touch Activation safeguards against cross-contamination • Consistent, unambiguous and simple Self-Screening or Supervised Screening • Most flexible installation options – perpendicular or parallel to the wall mounting or on a swing-away hinge to accommodate all facility needs • Unlike independent, dual pillar products, the portal configuration provides 18 detection zones as both sides communicate, maximizing sensitivity right in the middle • Unlike independent, dual pillar products, the portal configuration does not require constant re-alignment • Conforms to ES60601-1-8 international standards for medical device alarms (Does not cause alarm fatigue. No RED alarm lights, as color RED must be used ONLY in life threatening situations) • Conforms to IEC 60101-1:2005 medical device specification requirements (Ferromagnetic detectors are not considered to be medical devices; however, they are an integral part of the medical environment. As such, it is highly important that the power supply used in the detectors complies with standards for medical equipment used by the FDA, UL, as well as agencies around the world.)
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.
Symptoms: Flat or noisy ECG, frequent lead-off alarms.
Root cause: Worn electrodes, loose leads, or dry gel.
Symptoms: No pleth, SpO2 drops to --- or false low.
Root cause: LED/photodiode aging or cable damage.
Symptoms: Cuff fails to inflate, erroneous BP, long cycle.
Root cause: Pump/valve wear or cuff leak.
Symptoms: Dim, flickering, or unresponsive screen.
Root cause: Backlight or digitizer failure.
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.
High-turnover; keep inventory.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Rechargeable backup battery | Periodic replacement | $$ | Fairly easy |
| Display / touch assembly | Periodic replacement | $$$ | Difficult |
| ECG patient cable & lead set High-turnover; keep inventory. | Frequent wear item | $$ | Easy |
| SpO2 sensor (adult/ped/neo) | Frequent wear item | $$ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
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.
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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