
RTI Group North America · Model Cobia Dental
Li.li1 {margin: 0.0px 0.0px 0.0px 0.0px; font: 12.0px Carlito; color: #191c1f} span.s1 {font: 10.0px Symbol} span.s2 {background-color: #ffffff} ul.ul1 {list-style-type: disc} Easy to position with no position dependence Large, rotatable display Log/History function "Plug n Play" function Pulsed radiation analysis Full Auto range for kV, TF, and Sensitivity Bluetooth and USB communication Solid-state detectors = no need to compensate for temperature & pressure Built-in energy compensation Long-lasting rechargeable battery Always free firmware upgrades Up to ten-year warranty Two-year Calibration Cycle.
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.
Symptoms: Readings disagree with a reference standard, verification check outside tolerance.
Root cause: Normal drift - the instrument needs its scheduled factory / accredited calibration (at least every 12 months).
Symptoms: Dead unit, short battery life, will not charge.
Root cause: Depleted or aged battery, or a power / charger fault.
Symptoms: Open or intermittent readings, connection errors, a specific function fails.
Root cause: Worn or broken test leads, mains adapters, patient-lead adapters, or a sensor cable.
Symptoms: One parameter (leakage, insulation, ECG / SpO2 / IBP simulation, defib / pacer energy, ventilator flow / pressure, light / dose) errors or is out of range while others work.
Root cause: An internal source / measurement circuit fault on that channel.
Symptoms: The automation / logging software will not connect.
Root cause: USB cable / port or driver.
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.
At least every 12 months per the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Test-lead / adapter set | Periodic replacement | $$ | Easy |
| Battery | Periodic replacement | $$ | Easy |
| Calibration (factory / accredited) At least every 12 months per the manufacturer. | Frequent wear item | $$ | Easy |
| Communication cable | Periodic replacement | $ | Easy |
Relative cost: $ lowest · $$$$ 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 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.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Synced live from the FDA openFDA API.
Incorrect instructions for use (IFU) included.
RTI Surgical, Inc. of Alachua, FL is recalling their OPTEFORM Allograft Paste, 5cc as it may contain a 10 cc fluid dispenser. The 10cc fluid dispenser does not include the correct fluid fill line reference for reconstitution of 5cc past allografts.
From BioLab, for work done with this kind of equipment.
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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