Manufacturer of the MR diagnostic incubator system nomag®IC for MRI examination of premature and newborn infants
LMT Medical Systems GmbH
Lübeck (Headquarters) · USA (Subsidiary)New on Amplifa
About LMT Medical Systems
LMT Medical Systems GmbH, based in Lübeck, develops and manufactures the MR diagnostic incubator system nomag®IC Advanced, which allows premature and newborn infants to be transported directly from the neonatal intensive care unit to the MRI room and examined there non-invasively. The MR-conditional incubator continuously controls temperature and humidity in the patient compartment during transport and examination and is compatible with MRI systems from GE, Philips and Siemens. The portfolio also includes a 16-channel head coil and a 12-channel body coil for 1.5 and 3.0 Tesla, each specialized for neonatal imaging. The patented system has been in production since 2003 and is used in university hospitals worldwide; the approximately 20 employees at the Lübeck headquarters cover development, production and international sales. Since 2014, Geratherm Medical AG has been the majority shareholder; a US subsidiary serves US customers. Managing Director since the company's founding is graduate engineer Torsten Lönneker-Lammers.
- Site
- Lübeck
- Processes
- Development, Production, International Sales, Training/Product Support (Product Experts), Technical Documentation (Instructions for Use, Data Sheets)
- Certificates
- MDR (EU) 2017/745 conformity, notified body TÜV SÜD (0123), FDA approval, China certification, MDR (EU) 2017/745 – TÜV SÜD (0123)
- Employees
- 20
- Industries
- Medical technology, Radiology, Neonatology, Pediatric radiology
- 01
Development
- 02
Production
- 03
Technical Documentation
- 04
International Sales
- 05
Training/Product Support
Sites
Lübeck
DEHeadquarters: development, production, sales
Products
Inside the production
Industries
Additional services
Reference customers
Quality & Certification
The nomag®IC Advanced fully complies with Medical Device Regulation (EU) 2017/745 (MDR), certified by the notified body TÜV SÜD (0123), and is FDA approved; in addition, certification for China was obtained in 2021.
| Evidence | Lübeck |
|---|---|
| MDR (EU) 2017/745 – TÜV SÜD (0123) | |
| FDA approval | |
| China certification |
History
- 2003
Start of production of the MR diagnostic incubator system nomag®IC
- 2014
Geratherm Medical AG (Geschwenda/Thuringia) becomes majority shareholder
- 2021
Certification for China obtained
- 2025
nomag®IC Advanced fully compliant with Medical Device Regulation (EU) 2017/745 (MDR)