CE Marking
Compliance with Regulation (EU) 2017/745 (MDR) and, where applicable, Regulation (EU) 2017/746 (IVDR).
Medical Devices
From vital signs monitoring to advanced diagnostic systems — our medical device catalog covers every measurement your trial requires, calibrated and ready to deploy.
Comprehensive monitoring solutions for tracking vital signs and physiological measurements, supporting patient management, safety, and clinical data acquisition.
Measurement tools designed to assess key physical body parameters, including weight, height, and body composition, providing essential data for baseline assessment and ongoing patient monitoring.
Advanced cardiac monitoring solutions providing reliable, real-time data on key cardiovascular parameters to support diagnosis and patient monitoring.
Blood glucose measurement and continuous monitoring solutions, supporting diabetes management, glycemic control and metabolic health monitoring.
Solutions designed to safely deliver fluids, medications or nutrients into the body through controlled administration via various access routes, including intravenous, subcutaneous, intramuscular & neuraxial pathways.
Solutions for in vitro diagnostic testing, from central laboratories to point-of-care settings, enabling timely and reliable diagnostic insights.
Solutions for the acquisition, recording, and monitoring of neurophysiological, neuromuscular, and sleep-related physiological parameters.
Equipment supporting the measurement of physical performance, strength, endurance, pain, and functional abilities, facilitating the quantitative assessment of patient function and clinical outcomes.
Solutions for the assessment and monitoring of sensory and neurological function, ranging from sensory perception and sensitivity testing to comprehensive neurological evaluation.
Ophthalmology devices for visual function assessment and ocular care, from vision testing and refraction systems to diagnostic imaging and ophthalmic procedure equipment.
Technologies for real-time visualization and assessment of internal anatomical structures for diagnostic and procedural applications.
Specialized equipment for the assessment, monitoring, and evaluation of skin conditions and dermatological indications in clinical care and research applications.
Equipment supporting a wide range of respiratory applications, from pulmonary diagnostics and monitoring to therapeutic and respiratory support solutions.
Essential medical & pharmaceutical supplies supporting medication administration, patient care, and routine clinical operations across healthcare and research settings.
Our services
Each medical device goes through a rigorous preparation process before reaching your investigator sites — so your study can start without delay.
Calibration according to certified standards, with full traceability and calibration certificates.
Protocol-specific setup — parameters, units, alert thresholds — aligned with your study design. Devices arrive ready to use.
Devices configured in the appropriate language for each site, helping ensure smooth adoption and consistent use across your study.
Full functional inspection of every device before shipment to ensure it meets your protocol requirements.
User manuals in the correct language for each site. Documentation archived for 25 years with complete traceability through Quipsite.
Global delivery to investigator sites with real-time tracking. We handle customs, import requirements, and last-mile delivery.
Real-time visibility of equipment operations, complete traceability, and audit-ready documentation throughout your study.
Dedicated support throughout your trial — troubleshooting, replacement devices, on-site assistance. Response within 24h.
Certifications
Every device we supply is approved by the relevant regulatory bodies in the countries of use.
Compliance with Regulation (EU) 2017/745 (MDR) and, where applicable, Regulation (EU) 2017/746 (IVDR).
Compliance with applicable U.S. FDA medical device requirements, including 510(k) clearance, De Novo classification, or PMA approval, as applicable.
Compliance with the UK Medical Devices Regulations 2002 (SI 2002 No. 618, as amended).
Compliance with Canada's Medical Devices Regulations (SOR/98-282), including applicable MDL or MDEL requirements.
Compliance with Japan's Pharmaceuticals and Medical Devices Act (PMD Act).
Contact
Our team sources any medical device globally — even if it's not in our catalog. Tell us what your protocol requires and we'll find it. Response within 24 hours.
Easy there — at Quipment, every shipment is handled with care.