About usGet to know the IUL GROUP and its history
Since 1987 IUL is designing, producing, and commercializing automation solutions for microbiology laboratories. Our goals are: 1) to provide more comfortable, safer, and reliable microbiological control for the industry and 2) to deliver devices for in-vitro diagnostics in the field of human and animal health.
From the very beginning, IUL has been committed to research and innovation. In the last decade, IUL has opened its scope in the applications of light in Artificial Insemination, which improves fertility rates. IUL also designs, manufactures, and markets lateral flow readers for point-of-care, food, and environment for research and in-vitro diagnostics in the field of human and animal health. Both fields are taking more and more interest in the last years, becoming an essential part of the company.
A benchmark in Industry 4.0, IUL also develops OEM products for several companies, helping them achieve their objectives in a flexible manner and with the minimum time to market.
IUL, more than 30 Years of Experience
IUL, S.A. start
First instrument; Masticator homogenizer
Manual Colony Counter
Dosi Dilutor. Gravimetric dilutor
Haloes Caliper. Zone reader.
Countermat. First automatic colony counter.
Autosampler. First Robotic colony counter
Bio Dilutor. Serial Dilutions.
Delta Dilutor. Gravimetric diluter.
Eddy Jet & Mycrosyringe spiral plater.
Countermat Flash colony counter.
Polystainer slide stainer
Spin Air sampler
Plate Handler robotic colony counter
Flash&Go automatic colony counter
Pinch Dilutor gravimetric diluter
Smart Dilutor gravimetric diluter.
Phast Blue vPCR.
Eddy Jet 2.
From the very beginning IUL’s products have given creative solutions to everyday lab automation problems. With 15 international patents we are proud of our R+D capability.
Since 2003 IUL sets out the criteria for a quality management system certified ISO 9001. We believe in continual improvement to provide value to our organization.
All our products are CE certified, that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area.
FDA CFR 21 part 11
Our new instruments are compilant with CFR 21 part 11, that defines the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and equivalent to paper records
ISO 13485:2016 & EN ISO 13485:2016
IUL sets out the criteria for Medical Devices Quality Management