IVUS Medical ApS
The quality of a urine sample is determined long before it reaches the analyzer.
It starts with clear guidance, hygienic collection, correct sampling and secure preservation. At IVUS Medical, we develop products that support this process - because clean and correctly handled samples are essential for better diagnostics, fewer sources of error and more precise treatment.
Sampling Solutions Developed for Healthcare Professionals
IVUS Medical develops and manufactures medical devices and IVD products for hospitals, clinics and laboratories.
Our products are developed with a strong focus on quality, functionality and ease of use – based on the needs and challenges encountered in everyday clinical practice.
Several of our solutions have been developed in close collaboration with healthcare professionals to make the collection and handling of biological samples as safe, simple and efficient as possible.
Urine Collection
Sterile urine collection kits with specially designed containers for safe and hygienic urine sampling. The kits are individually packed in easy-to-open peel pouches for convenient handling in clinical practice.
Vacuum Urine Collection
Closed vacuum collection systems designed for hygienic transfer of urine samples from the collection container directly into a vacuum tube. The closed transfer helps minimise contact with the sample and reduces the risk of spillage during handling.
Sample Tubes
Sterile sample tubes for the collection, handling and transport of biopsies, cerebrospinal fluid and other biological samples. The tubes are individually packed in easy-to-open peel pouches for convenient handling in clinical practice.
Meeting the Highest Standards
Quality Throughout the Process
As a manufacturer, IVUS Medical works systematically with quality throughout the entire product lifecycle – from product development and material selection to production, documentation and ongoing quality assurance.
IVUS Medical is certified according to:
ISO 13485 · ISO 9001 · ISO 14001
Our IVD products are CE marked and comply with the applicable requirements of the EU In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR).
