B Medical Systems S.a r.l.
Luxembourg medical cold-chain equipment manufacturer.
B Medical Systems manufactures medical refrigerators, vaccine freezers, transport boxes, and blood-management cold-chain equipment. Founded in Luxembourg in 1979, the company supplies health systems, NGOs, laboratories, and distributors worldwide.
- Type
- Manufacturer
- Location
- Hosingen, Luxembourg
- Founded
- 1979
- Website
- bmedicalsystems.com
- Categories
- Medical & Healthcare Supplies, Electrical & Power Equipment
- Markets
- Luxembourg, Germany, United States, India
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
- domain-registered (green), checked 2026-08-06 Domain registry record
- sanctions-clear (green), checked 2026-08-06 OpenSanctions
- debarment-clear (green), checked 2026-08-06 OpenSanctions
- public-contract-awarded (green), checked 2026-08-23 TED, EU public procurement bulletin Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)