Patient Monitoring & Infusion

Monitoring clinicians trust at the bedside

Bedside, transport and infusion systems built for continuous use across intensive care, operating theatre and emergency departments.

Nurse checking a bedside patient monitor in a daylit intensive care unit
A bedside monitor on its rolling stand in an ICU bay — the configuration described under Intensive care below.
Europe
CE marked, EU MDR
United States
FDA 510(k) cleared
Quality system
ISO 13485 certified
Registered markets
42 countries

Market Access

Where our devices are registered

42

markets with an active registration or an accepted submission.

Regulatory status by region
RegionFrameworkDevice classReferenceStatus
European UnionEU MDR 2017/745Class IIa / IIbNB 0123 · CE 748291Registered
United StatesFDA 510(k)Class IIK243117Cleared
United KingdomUKCAClass IIaAB 0086 · UK 31204Registered
BrazilANVISA RDC 751Class IIISubmission 25351.204Under review
Gulf statesSFDA / MOHAPClass B / CMDMA-2024-1187Registered
Southeast AsiaASEAN AMDDClass B / CSG DE-0442Registered

Quality system ISO 13485:2016, certificate 0123-QS-1180, issued by notified body 0123. Reference numbers shown are specimen values for this demonstration — replace with the issued certificate, clearance and registration numbers before publication so buyers can verify them independently.

By Department

Configured for the ward it runs in

Patient monitor and infusion pump at an intensive care bedside Anaesthesia and monitoring equipment beside an operating table Portable transport monitor on a trolley in a hospital emergency department
Intensive care

Intensive care

Twelve-hour shifts with no gap in the trace, and alarm limits a nurse can retune without leaving the bed.

  • KM-780 Bedside Monitor 12.1 in display8 parameters72 h trend storage
  • KV-320 Infusion Pump 0.1–1200 mL/h±2% accuracyDose error reduction
  • KM-780C Central Station Up to 32 beds96 h full disclosure
See the ICU configuration

Operating theatre

Haemodynamics, gas and depth of anaesthesia readable from across the table, on one screen.

  • KM-780 OR Configuration Anaesthetic gas moduleDual IBPCeiling or rail mount
  • KV-320 Infusion Pump TCI-ready protocols4-pump stacking
See the theatre configuration

Emergency & transport

Handover from ambulance to resuscitation bay without a break in the recorded trace.

  • KT-150 Transport Monitor 4.5 h battery2.9 kgIP44 rated
  • KM-780 Bedside Monitor Docked handoverContinuous trend transfer
See the emergency configuration

Product Selector

Compare models and check availability

ModelKey parametersWard fit Regulatory classAvailabilityDetails
KM-780 bedside monitor on a rolling standKM-780Bedside monitor 12.1 in display8 parameters 5.4 kg 5–40 °C ICU · ORIIa (EU) · II (US)Stocked · 6–8 weeks Specifications
KM-780C central station display on a desk standKM-780CCentral station 24 in displayUp to 32 beds 7.8 kg 5–40 °C ICUIIa (EU) · II (US)Built to order · 10–12 weeks Specifications
KV-320 volumetric infusion pump on a pole clampKV-320Volumetric infusion pump 0.1–1200 mL/h±2% accuracy 2.1 kg 5–40 °C ICU · OR · EDIIb (EU) · II (US)Stocked · 4–6 weeks Specifications
KT-150 portable transport monitor with a carry handleKT-150Transport monitor 4.5 h batteryIP44 rated 2.9 kg −10–40 °C ED · TransportIIa (EU) · II (US)Stocked · 6–8 weeks Specifications

Full specifications and instructions for use are published as HTML pages — no registration, no gated download. PDF datasheets are offered alongside them, not instead of them.

Technician in cleanroom garments assembling a medical device board at a lit workstation

Quality System

Traceable from board to bedside

Every unit we ship can be traced back to the batch it came from and the tests it passed. That record is what a hospital audit asks for, and what a recall would depend on.

  • ISO 13485 design control

    Every change is documented from design input through to release.

  • UDI-level traceability

    Each unit maps to its batch, components and final test record.

  • Post-market surveillance

    Field complaints feed back into the next hardware revision.

Field service engineer commissioning a patient monitor at an empty hospital bedside with a laptop on the bed tray
Commissioning on the ward before handover — every unit is verified against the configuration you ordered, not against a demo profile.

After Delivery

What happens after the shipment lands

  1. 01

    Installation & commissioning

    Our engineer verifies every unit on site before handover.

  2. 02

    Clinical training

    Ward teams are trained on the exact configuration you bought.

  3. 03

    Preventive maintenance

    Scheduled checks with loaner units, so beds stay covered.

  4. 04

    Spare parts & consumables

    Cables, sensors and sets supplied for ten years after purchase.

Get a Configuration

Tell us which ward you are equipping

Send the ward type and bed count. We come back with a configuration, lead time and quotation within two business days — no account, no form wall.

Request a quotation
Regulatory affairs
ra@kelvara-medical.example
Registered office
Wilhelminakade 173, 3072 AP Rotterdam, Netherlands
EU authorised rep
Required under EU MDR — insert EC REP name and address before publication

Contact details on this page are demonstration placeholders. Replace the phone number, addresses and EC REP details with the real entity before publication — a visibly placeholder number damages trust more than showing none.