Radiometer ABL700
Radiometer · Model ABL700
Unique technology eliminates the interfering effects some substances have on the accuracy of blood gas, oximetry, glucose, and lactate measurements. Save time with automation of work processes. Auto Check quality control module automates and improves quality control procedures. Remote and automated management of patient and analyzer data from a central location through RADIANCE STAT analyzer management system software. Automatic accession number request to LIS (Laboratory Information System). Flexible setup options to fit different needs. Simplify your routines. Simple and intuitive sample analysis procedures. Online help function with interactive video tutorials.
Key tips
- ·Run QC controls before trusting any repair - an analyzer that passes self-test can still report clinically wrong results.
- ·Rule out a reagent lot change before opening the instrument - it can look exactly like a hardware fault.
- ·Centrifuge rotors have a hard retirement age/cycle limit regardless of visible condition - don't eyeball it.
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.
Sensor / electrode fault or drift
HighSymptoms: pH, pCO2, pO2, electrolyte, glucose / lactate or CO-oximetry results flagged, QC fails, stability / response errors.
Root cause: An electrode / membrane at end of life, an air bubble or protein in the measuring path, or a calibration fault.
Sample-path / inlet clog or clot
MediumSymptoms: Sample not aspirated, clot detected, inlet / preheater alarm.
Root cause: Clot in the inlet probe / preheater, or a worn inlet gasket.
Solution / cartridge / gas / waste fault
MediumSymptoms: Reagent-empty, gas-supply or waste-full alarm, calibration fails.
Root cause: Empty or expired solution pack / cartridge, an empty / expired gas cylinder, or a full waste container.
Pump / valve / pneumatic fault
MediumSymptoms: Poor sample transport, calibration or rinse failures, pressure alarms.
Root cause: Worn peristaltic pump tubing, a pinch-valve fault, or a pneumatic-pressure fault.
CO-oximetry / optical fault
MediumSymptoms: tHb, sO2 or dyshaemoglobin results implausible, optics / lamp error.
Root cause: Optics contamination, a lamp fault, or the haemolyser.
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.
Sensor cassette / individual electrodes & membranes
Class Frequent wear itemRel. cost $$$R&R Fairly easy
Solution pack / reagent cartridge
Class ConsumableRel. cost $$R&R Easy
Calibration gas cylinder
Class Frequent wear itemRel. cost $$R&R Easy
Peristaltic pump tubing / pinch valves
Class Frequent wear itemRel. cost $R&R Moderate
Inlet probe / preheater gasket
Class Frequent wear itemRel. cost $R&R Fairly easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Sensor cassette / individual electrodes & membranes | Frequent wear item | $$$ | Fairly easy |
| Solution pack / reagent cartridge | Consumable | $$ | Easy |
| Calibration gas cylinder | Frequent wear item | $$ | Easy |
| Peristaltic pump tubing / pinch valves | Frequent wear item | $ | Moderate |
| Inlet probe / preheater gasket | Frequent wear item | $ | 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.
- ·Daily QC controls run and reviewed
- ·Calibration verification per assay
- ·Routine cleaning and decontamination
- ·Scheduled reagent-path and pump-tubing maintenance
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: Sensor / electrode fault or drift / QC failure
- Run the relevant calibration and check the sensor / electrode status screen.
- De-bubble / rinse the measuring path and check for protein deposits.
- Replace an electrode / membrane / sensor cassette at end of life or that fails calibration.
- Confirm the solution pack / reagent cartridge and calibration gas are in date and not empty.
- Re-run QC at the relevant levels before releasing results.
Symptom: Sample not aspirated / clot / inlet alarm
- Run the inlet / preheater clot-removal or rinse routine.
- Inspect the inlet probe and gasket.
- Replace the inlet gasket or probe.
- Confirm free sample aspiration with a QC sample.
- Replace worn peristaltic pump tubing if transport is still poor.
Symptom: Result flagged / questionable vs the clinical picture
- Repeat with a fresh sample / strip / cassette from correctly stored, in-date stock.
- Run the QC controls at each level.
- Confirm the meter / analyzer is coded / calibrated to the current lot.
- Clean the measurement chamber / strip port and the optics per the manual.
- Quarantine the lot if QC fails; refer the analyzer if QC passes but a result still looks wrong.
Symptom: Will not power on / short battery life / strip-port fault (handhelds)
- Fit fresh batteries or confirm the charger / dock.
- Clean the strip-port contacts / optics.
- Try several strips from a fresh vial.
- Replace the battery.
- Replace the meter if it will not read known-good strips.
Technical Specs
- Height
- 440 cm
- Length
- 530 cm
- Weight
- 30.3 – 32.6 kg
- Width
- 700 cm
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Central / core laboratory
- Point-of-care testing stations
- Blood bank
- Microbiology lab
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
A customer has reported an error on an ABL8xx configured to a Hospital Information System using the data transfer protocol HL7 version 2.5. If the instrument transmits results to a HIS system and the connection is broken the results are queued for later transmission. If the ABL and HIS system are configured with HL7 2.5, any results in the queue will be mixed up when the instrument transmits t
- RECALL
Based on internal testing and user/customer complaint reports received, the firm determined that wrinkles may arise on the outer membrane of the calcium membrane units upon installation. Retention of fluids between the wrinkles can cause a positive bias resulting in calcium measuring errors. This situation poses a risk to the safety of patients, particularly when the measurement results are used
- RECALL
Reported calibration errors are not displayed on the analyzers parameter bar screen or on the patient results when the calibration number is between 32768 - 65535 and 98303 - 131070. This may cause the operator to perform measurements and obtain questionable results.
- RECALL
An increased failure rate was observed with the yellow rubber tubing. The tubing was found to be leaking blood and solutions after distribution.
- RECALL
Calibration solution for ABL700 Blood Gas Analyzers is labeled with an incorrect bar code. The bar code identified on the Cal Solution 2 product is actually the bar code for the rinse solution.
- RECALL
The CI membrane units generate too low values for status and sensitivity during calibration.
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