Parks · Model Flo-Lab 2100-SX
• Tops in Testing Capabilities • Better Studies in Less Time • Designed to help you focus on performing the fastest, most accurate studies on all of your patients, even those with severe disease. • Most accurate in the world-and the most flexible, user-friendly operation of any vascular system. • Performs a full range of lower arterial, upper arterial, and venous studies, providing complete vascular diagnostic services for your patients.
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: Weak, absent, or noisy Doppler signal.
Root cause: Probe crystal or cable wear.
Symptoms: Inaccurate or failed pressure readings.
Root cause: Cracked cuff bladder or tubing/connector leak.
Symptoms: Distorted or flat plethysmography waveform.
Root cause: Pneumatic transducer calibration drift.
Symptoms: Incorrect ABI/TBI calculation, or frozen screen.
Root cause: Application software or workstation fault.
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 spares.
Consumable; multiple sizes.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Pneumatic tubing / connector set | Periodic replacement | $$ | Fairly easy |
| Workstation / PC | Major service part | $$$ | Moderate |
| Doppler probe High-turnover; keep spares. | Periodic replacement | $$$ | Fairly easy |
| Blood pressure cuff set Consumable; multiple sizes. | Periodic replacement | $ | Easy |
Relative cost: $ lowest · $$$$ 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 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.
Synced live from the FDA openFDA API.
Parks Medical Electronics, Inc. was made aware of two incidents where an air supply tube from their PARKS PVR unit was inadvertently connected to an IV in the patient's arm instead of into the blood pressure cuff.
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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