Aura PCR — main photograph
BioAirAvailability: Supplied to order

Aura PCR

Reference aura-pcr

These state-of-the-art PCR cabinets are specially designed for pre- amplification sample preparation in controlled environment in order to prevent DNA carry-over. Any aerosol generated during the handling of the post amplification samples cannot enter the cupboard; any molecule of DNA herein contained is subsequently neutralised with the help of UV radiations.

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At a glance

Reference
aura-pcr
Category
Biosafety Cabinets & Laminar Flow
Equipment family
DNA cross-contamination control enclosure

Overview

These state-of-the-art PCR cabinets are specially designed for pre- amplification sample preparation in controlled environment in order to prevent DNA carry-over. Any aerosol generated during the handling of the post amplification samples cannot enter the cupboard; any molecule of DNA herein contained is subsequently neutralised with the help of UV radiations.

Maintenance contract — AxiTech provides planned preventive maintenance for Aura PCR from BioAir: scheduled visits, safety checks, periodic calibration and a documented service report, backed by a contractual response time.

Troubleshooting, repair and spare parts — our biosafety cabinets & laminar flow engineers diagnose and repair Aura PCR on site or in the workshop, fit genuine spare parts and recommission the equipment after performance verification.

Features

  • Passive PCR enclosure (non ventilated)
  • Fluorescent light turns on automatically when opening the front glass or when UV lights turn off (user selectable)
  • Digital timer for UV lights with memory of the last setpoint
  • 100% UV-safe
  • Front glass divided in three hinged sectors
  • Internal foldable shelf in glass
  • Working surface in chemical resistant polyethylene
Service coverage

AxiTech maintains, repairs and supplies this equipment for hospitals, clinics, laboratories and imaging centres.

Maintenance contracts for Aura PCR

AxiTech provides preventive maintenance contracts for Aura PCR. Each contract fixes a schedule of planned visits in which our biomedical engineers inspect the equipment, replace wear parts before they fail, and verify that it still performs inside the manufacturer’s tolerances.

Every visit includes calibration and performance verification, and closes with a documented maintenance report you can present during an accreditation audit. Spare-parts availability and a guaranteed response time are written into the contract, so a breakdown never leaves a department waiting for an answer.

Plan at least one preventive maintenance visit per year, and a second visit for equipment in continuous or critical use.

  • Planned preventive maintenance visits at a fixed interval
  • Calibration and performance verification against the manufacturer’s specifications
  • A documented maintenance report after every intervention
  • Guaranteed availability of spare parts and consumables
  • A contractual response time when the equipment fails

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Planned preventive maintenance and calibration under contract

Troubleshooting and repair for Aura PCR

When Aura PCR fails, our engineers start with a structured diagnostic: error codes, electrical and mechanical checks, and a functional test against the equipment’s own specification. That tells us whether the fault is a consumable, a worn part or a board-level failure before any part is ordered.

Straightforward faults are repaired on site so the department loses as little time as possible. Anything that needs a workbench, a full strip-down or a specialised spare part goes to our workshop and comes back only after a complete post-repair test and, where the equipment requires it, recalibration.

Faults we see most often on this type of equipment

The faults we see most often are worn moving parts, power-supply and control-board failures, sensors that have drifted out of tolerance, and fluid or air paths that have become blocked or contaminated.

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Diagnostics, corrective repair and spare parts in the workshop
Troubleshooting

How to troubleshoot Aura PCR

Work through these checks before you escalate. They are the same first-line sequence our biomedical engineers run on arrival, and they either clear the fault or narrow it down enough that the intervention starts with the right spare part in the van.

  1. Capture the fault before you touch anything: write down the exact error code or message, the serial number from the rating plate, what the operator was doing and whether the fault clears on a restart.

  2. Confirm the power supply end to end — wall outlet, mains lead, fuse and any UPS or stabiliser in between. A device that is intermittently dead has a supply fault far more often than an internal one.

  3. Check the consumables and wear parts — filters, seals, tubing, probes, batteries — and note when each was last replaced. Anything past its service interval is the first suspect.

  4. Reproduce the fault once, deliberately, and record the sequence: what the operator did, what the device displayed, and whether a full power cycle clears it.

  5. If the fault is still there, escalate with the evidence. Send AxiTech the model, serial number, error code and the checks you have already run, and an engineer will come back with a diagnosis, a repair quote and a spare-parts lead time for Aura PCR.

What to send us when you report the fault

  • Manufacturer, model and serial number, from the rating plate
  • The exact error code or message, and the screen it appears on
  • When the fault started, how often it occurs and what triggers it
  • A photograph of the display or of the fault, and the last maintenance report

If the fault survives all five steps, stop using Aura PCR and open a repair request. Continuing to run equipment through a fault it cannot clear turns a component failure into a board-level one, and on devices used for diagnosis or therapy it puts the result — and the patient — in doubt.

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Buying and installing Aura PCR

AxiTech supplies Aura PCR together with the accessories and consumables it needs to enter service. We handle importation, delivery and installation, then commission the equipment on site so that it is verified against its specification before the first patient or the first sample.

Installation is followed by training for the users and for your biomedical team, warranty registration, and — if you want it — a maintenance contract that takes over the day the warranty ends, so the equipment never spends a period without planned service.

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Delivery, installation, commissioning and user training
Questions we are asked

Frequently asked questions about BioAir Aura PCR

Yes. AxiTech services Aura PCR, either under a maintenance contract or as a one-off intervention. Our biomedical engineers cover preventive maintenance, calibration, corrective repair and spare-parts supply for this equipment.

Other BioAir equipment we supply, install and maintain.