GE VINGMED ULTRASOUND AS

Listed in a source registry

Norway Brønnøysund Register Centre (brreg.no)

Verified facts

• ownership-on-record (green), checked 2026-08-13 GLEIF global LEI index
• registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
• lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
• annual-accounts-filed (green), checked 2026-08-14 Regnskapsregisteret (Brønnøysundregistrene, annual accounts)

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)

Check independently

• Sanctions and watchlists (OpenSanctions)