What happens to a bed between two patients
Rental equipment has been in someone else's home. That is the part nobody in this industry wants to talk about, so here is our process in full — including what we do not claim.
- 1
Strip and inspect on collection
Linen, mattresses, cannulae, masks and tubing are removed at the patient's address, bagged and never travel with the frame. Single-patient consumables are disposed of, not reissued.
- 2
Detergent wash
Every surface the patient or carer touches — frame, rails, controls, castors, handsets — is washed with a neutral detergent solution to remove organic soil. Cleaning has to happen before disinfection; disinfectant applied over soil does not work.
- 3
Disinfection to the manufacturer's instructions
Each device is disinfected using the agent, dilution and contact time its own manufacturer specifies for reprocessing. Different plastics and coatings tolerate different chemistry, so we follow the device's instructions rather than applying one product to everything.
- 4
Consumables replaced, not cleaned
Nasal cannulae, BiPAP masks and cushions, humidifier chambers, suction catheters and ECG electrodes are replaced with new items for every issue. These are not reprocessed under any circumstances.
- 5
Functional test and calibration check
Motors, brakes, alarms, flow rates and pressures are tested against specification before the unit is cleared. Oxygen concentrators are checked for output purity; monitors are checked against a reference.
- 6
Sealed, logged and handed over
The unit is sealed and logged against a checklist that lists the date, the technician and each step completed. That checklist is handed to you at delivery — you should not have to take the process on faith.
What we do claim
- · Reprocessing follows each device manufacturer's own instructions.
- · A dated, signed checklist accompanies every rental unit.
- · Patient-contact consumables are new for every issue.
- · Devices are function-tested against specification before dispatch.
- · Equipment is sourced from established manufacturers holding the licences applicable to their device class.
What we do not claim
- · We are not ISO 13485 certified — that standard applies to device manufacturers.
- · We are not “CDSCO approved” — CDSCO does not license rental providers.
- · We hold no ICMED certification and are not an AiMeD member.
- · Our equipment is not sterile. It is cleaned and disinfected, which is the correct standard for reusable non-critical devices — not the same thing as sterilisation.