Cyclic ProDX™
"This is a game-changer" IVF nurse of 25 years
Hormone monitoring is critical to fertility treatments from adjusting doses to timing key events during treatment.
The Cyclic ProDX platform enables clinicians to get hormone results quickly, in minutes, allowing fast treatment decisions and face to face communication with the patient while they are still in the clinic.
Fast, efficient testing
The Cyclic ProDX has four test channels allowing the measurement of 4 samples in parallel, and 12 per hour with a single analyser
Highly-intuitive user interface
Designed to be simple to use by any trained healthcare worker. Load the sample onto the cartridge, insert into the analyser and start the automated measurement.
As simple as 1-2-3
- Sample collection
- Sample processing
- Testing with Cyclic ProDX (15 mins)
Technical specification
Unique technology for accurate, rapid testing of hormones in clinic
Detection: | Quantitative fluorescence |
Channels: | 4 incubation+test channels & 1 additional test channel |
Incubation: | 32°C isothermal incubation environment |
Dimensions: | 30 cm (W) x 28 cm (D) x 15 cm (H) |
Weight: | 4 kg |
Regulatory approval: | CE |
Intended use: | Professional use only |
Languages: | English & Spanish |
Download the specs
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Frequently Asked Questions
If you have any other questions, get in touch to speak to a member of our sales team.
No, individual clinics performing testing in-house do not require UKAS accreditation. UKAS accredits calibration and testing services so laboratory service companies require UKAS accreditation.
Not at all! We'll get you set up with an analyser and the tests that you want to run and with those in place we can have you up and running in a couple of hours.
Medical devices and in vitro diagnostics (IVDs) are required to be CE-marked and, ideally, are manufactured in an ISO 13485 certified manufacturing facility which ensures that the highest quality standards are met throughout the manufacturing process. In the UK, medical devices and IVDs are required to be registered with the MHRA before being placed into the UK market. Cyclic ProDX is CE-marked, registered with the MHRA and is manufactured in an ISO 13485 certified facility.
The HFEA has confirmed with us that it doesn’t place specific requirements on IVDs being used within IVF clinics, however clinics continue to be obliged to follow standard licence conditions (SLC) where T30 stipulates to use CE marked, CE and UK(NI) marked or UKCA marked medical devices wherever possible. Additionally, Guidance Note 26 in the HFEA Code of Practice outlines the requirements for Equipment and Materials which should be adhered to. Clinics can also get in touch with their HFEA inspector if they have any questions on this matter.