Near-painless, with a cleaner heal.
No needle, no anticipatory anxiety. The laser cauterises as it lances, lowering infection risk and speeding healing — particularly valuable in paediatric, diabetic and frequent-draw contexts.
UK distributor · MHRA-registered medical device
Lancing,
without the
lance.
HandyRay-Pro replaces the disposable needle with a medical-grade 3R laser. A single device that performs up to 50,000 lances, produces zero sharps waste, and removes the moment patients dread most from routine blood testing.
01 · The device
HandyRay-Pro.
One device.
No sharps.
A handheld, clinical-grade 3R laser lancing device. Replaces decades of single-use steel and plastic with a single rechargeable instrument: fast, near-painless, and engineered for repeated daily use in clinical workflows.
- Classification
- Class IIa
- Laser class
- 3R, 905 nm
- Lances per unit
- Up to 50,000
- Cycle time
- ~2 s
- Sharps waste
- 0 g
- UK distributor
- Medenico Ltd.
Optics
Calibrated 3R laser optics. Skin contact triggers the cycle automatically.
Depth control
Adjustable depth and sample volume across paediatric, adult and venous draws.
Sterile by design
Non-contact emission removes cross-contamination risk and disposal overhead.
Also in the range
HandyRay-Lite, for personal and home use.
02 · The case for switching
Better for
patients.
Better for budgets.
Steel-and-plastic lancing is a hidden cost-centre in every clinic: procurement, handling, sharps disposal, needlestick risk. HandyRay-Pro folds that whole chain into one device, with a clinical experience patients prefer.
Zero sharps waste.
Removes the entire single-use lancet stream, along with the disposal, training and audit 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.
BY THE NUMBERS
One device.
A measurable shift.
Modelled against a mid-size diabetes clinic running ~120 lances per day, over a five-year window.
0
LANCES PER UNIT
Upper bound, per device. 30,000 guaranteed.
0%
LESS PLASTIC & STEEL WASTE
vs. equivalent single-use lancet volume.
0
NEEDLESTICK INJURIES
No sharps in the workflow. Zero by design.
03 · UKRP services
Your post-Brexit
UK Responsible
Person.
For overseas manufacturers placing medical devices on the UK market, Medenico operates as your registered UKRP. We handle MHRA registration, vigilance reporting, labelling review and ongoing compliance, end to end.
-
MHRA device registration
All risk classes, including Class I, IIa, IIb and III devices. UDI, GMDN and IVDR alignment.
-
Vigilance & post-market surveillance
Incident reporting, FSCA management, and ongoing surveillance reporting to the MHRA on your behalf.
-
Labelling & UK-language review
IFU, labelling and packaging review for UK regulatory and language requirements pre-launch.
-
Technical file & audit liaison
A single, accountable UK address for documentation, audit response and Competent Authority correspondence.
04 · Get in touch
Talk to
Medenico.
Clinical evaluation, procurement, or UKRP engagement: tell us which and we'll route you to the right team within one working day.
Clinical & procurement
info@medenico.comUKRP / regulatory
regulatory@medenico.comTelephone
+44 (0) 1732 617 850Office
1 Webbs Court, Buckhurst AvenueSevenoaks, Kent · TN13 1LZ