Near-painless, faster healing.
No needle, no anxiety. The laser cauterises as it lances, lowering infection risk and accelerating the healing process.
Lancing without
the needle.
HandyRay-Pro draws capillary blood with a medical-grade 3R laser instead of a disposable lancet. One rechargeable device performs up to 50,000 lances, produces no sharps waste, and spares patients the needle.
One device.
No sharps.
A handheld 3R laser lancing device that does the job of the single-use steel lancet. One rechargeable instrument: quick, near-painless, and built for repeated daily use in a clinical workflow.
- Class IIa medical device, made by LaMeditech (Republic of Korea) and distributed in the UK by Medenico.
- Replaces up to 50,000 single-use lancets per unit.
- For NHS Trusts, private clinics and home use.
Optics
A calibrated 3R laser. Skin contact triggers the cycle automatically.
Depth control
Adjustable strength and sample volume. Safe for paediatrics and adults.
Sterile by design
No cross-contamination, no needle stick injuries.
Also in the range
HandyRay-Lite, for personal and home use.
Why switch
Better for patients.
Better for budgets.
Single-use lancing carries hidden costs in every clinic: procurement, handling, sharps disposal and needlestick risk. HandyRay-Pro replaces that whole chain with one device, and gives patients a better experience at the point of testing.
Zero sharps waste.
Removes the entire single-use lancet waste stream, along with the disposal costs and overhead that comes with it.
No needlestick risk.
A non-contact device removes the leading cause of clinical-staff injury at the point of testing.
One unit, five years.
A single HandyRay-Pro replaces tens of thousands of consumables across a typical clinic lifecycle.
UKRP services
Your UK Responsible
Person, post-Brexit.
For overseas manufacturers placing medical devices on the UK market, Medenico acts as the registered UK Responsible Person. We handle MHRA registration, vigilance reporting, labelling review and ongoing compliance, end to end.
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MHRA device registration
All risk classes, including Class I, IIa, IIb and III devices. UDI, GMDN and IVDR alignment.
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Vigilance & post-market surveillance
Incident reporting, FSCA management, and ongoing surveillance reporting to the MHRA on your behalf.
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Labelling & UK-language review
IFU, labelling and packaging review for UK regulatory and language requirements pre-launch.
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Technical file & audit liaison
A single, accountable UK address for documentation, audit response and Competent Authority correspondence.
Get in touch
Talk to Medenico.
Clinical evaluation, procurement, clinical evidence or UKRP engagement: tell us which and we will point you to the right team, usually within one working day.