Preventive Maintenance
Scheduled PM programs with full documentation, built for Joint Commission and CMS survey readiness. Intervals set to manufacturer recommendations and your risk profile.
Independent biomedical equipment maintenance, repair, and calibration for hospitals, surgery centers, dialysis clinics, and physician practices.
Contract or per-event. Every service line produces a written record you can hand to a surveyor.
Scheduled PM programs with full documentation, built for Joint Commission and CMS survey readiness. Intervals set to manufacturer recommendations and your risk profile.
Fault diagnosis and repair on-site at your facility. We report root cause, parts replaced, and post-repair verification results, not just “resolved.”
Performance verification and electrical safety testing to manufacturer specification, with as-found and as-left values recorded on every device.
Preventive and corrective support for Prismaflex CRRT systems, performed by a technician with manufacturer-specific training and certification on the platform.
De-install, transport, re-commission, verify. Moves between suites, floors, or buildings without leaving a device in unverified condition.
Asset inventory, service history tracking, and repair-versus-replace guidance so capital requests are backed by your own device data.
Don’t see your equipment? Ask.
Send us the make and model →OEMs are the correct choice for devices under warranty, for proprietary software and firmware work, and for late-stage imaging and other high-complexity platforms. For general biomedical equipment, an independent organization is usually faster, cheaper, and easier to work with. Here is the honest comparison.
Runtime Biomed is owner-operated. The work is performed by a biomedical engineer and clinical engineering technician currently working in a hospital environment, supporting preventive and corrective maintenance, troubleshooting, equipment inspections, and documentation across a mixed clinical fleet.
That includes specialized training and certification on the Prismaflex CRRT system, plus hands-on experience with infusion pumps, patient monitoring equipment, defibrillators, feeding pumps, blood warmers, and other clinical equipment. The person you call is the person who shows up.
Smaller clinics and healthcare facilities without dedicated in-house clinical engineering resources, plus larger sites that need overflow capacity on a mixed-vendor fleet.
The same sequence every time, whether it is an emergency or a scheduled PM visit. You always know what happens next and what you receive at the end.
Call the service line or submit the form with the device, location, and symptoms. Emergencies go by phone so nothing waits in an inbox.
We confirm the model, likely fault, and whether parts are on hand, then agree the visit window and what access we need.
On-site diagnosis, repair, calibration, and post-service verification. If the fault turns out to belong with the manufacturer, we say so before spending your money.
You receive the completed work order with findings, parts, test values, and technician detail, ready for your CMMS or survey binder.
No multi-year lock-in and no minimum fleet size. Start with one device or one audit; scope is quoted per facility once we see the asset list.
A walk-through of your devices with a written condition report: what is due, what is failing, what is out of specification, and what needs attention first.
Build or correct the asset list (make, model, serial, location, ownership, and service status) so you know what you actually have before you plan around it.
Set up PM intervals, service records, and a filing structure that holds up under a Joint Commission or CMS survey rather than being assembled the week before.
Remote or on-site help on a specific fault, alarm, or intermittent issue, including a straight answer on whether it is worth repairing.
Repair-versus-replace analysis and specification support before a purchase, so capital requests are backed by device data rather than a vendor quote.
A standing arrangement covering scheduled PM, corrective calls, and record-keeping for facilities with no in-house clinical engineering.
Platform-specific PM and corrective service for Prismaflex CRRT systems, backed by manufacturer training and certification.
Every item here is something we can produce paperwork for on request: scope, coverage, agreements, and qualifications. Nothing on this page is a claim without a document behind it.
We perform servicing: maintenance, repair, and calibration that returns a device to its original specifications. We do not remanufacture. Scope is stated consistently with FDA’s 2024 final guidance on servicing versus remanufacturing.
General liability and professional liability coverage in place. A certificate of insurance is furnished on request and can be issued naming your facility before the first service event.
A BAA is available and can be executed before the first service event for any device that stores or transmits PHI.
Prepared to enroll and maintain compliance through Symplr and IntelliCentrics, including immunization records, training, and background screening for site access.
Work order, device identifiers, findings, parts used, test equipment referenced, as-found and as-left values, technician, and date, formatted to drop into your CMMS or survey binder.
Biomedical engineer and clinical engineering technician working in a hospital environment, with manufacturer training and certification on the Prismaflex CRRT system.
Territory is deliberately tight. A regional footprint is what makes a same-day site visit realistic instead of aspirational.
Emergency calls are answered outside these hours. Scheduled work is booked inside them, weekends included.
Outside these areas? Ask. We travel across the DMV and surrounding areas →
Eight questions facilities ask before signing anything. If yours is not here, the phone line answers it faster than a form will.
Devices still under manufacturer warranty should stay with the OEM, and we will tell you when that applies. Outside of warranty, servicing by a qualified independent organization is a normal and permitted practice. We document scope so your records show servicing to original specification, not modification.
OEM parts through authorized channels wherever they are available to us. When a part is only obtainable as tested pre-owned or third-party equivalent, we tell you before ordering and note it on the work order. Never silently.
Response commitments are written into your agreement, set per urgency tier, rather than advertised as a fleet-wide average. Emergency calls go to the phone line and are triaged the same day; scheduled work is booked to a window you agree in advance.
No. CT, MRI, fluoroscopy, and comparable high-complexity imaging platforms belong with the OEM or an imaging specialist. We will point you to the right party rather than take the ticket.
Yes. Work orders are delivered in a consistent format with device identifiers, dates, findings, parts, and as-found / as-left values, so they can be attached to or imported into whichever system you keep records in. Tell us the format your CMMS expects and we will match it.
Yes. Prismaflex CRRT is a platform we hold specific manufacturer training and certification on, covering both preventive and corrective service. For other CRRT platforms, ask, and we will tell you plainly whether it is in scope.
With an assessment and an asset audit. Most facilities in that position do not have a reliable device list, so the first visit produces one, along with a written view of what is overdue, failing, or out of specification.
No. Small facilities are the reason this exists. A two-device exam room and a twelve-suite surgery center get the same documentation package.
Device down and affecting patient care? Call. Don’t use the form. Answered seven days a week.
(443) 866-5426Open 7 days · emergency calls taken outside these hours