GE VINGMED ULTRASOUND AS
No description from the company. The catalog line you may see elsewhere is generated by us from the category and location, not a statement by the company.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Horten, Norway
- Founded
- 1985 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- https://www.gehealthcare.com
- Categories
- Artykuły medyczne i związane z opieką zdrowotną
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 13 official records from 12 official sources are on file. 4 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Active legal entity ID (LEI) (record type: lei-active) [official record; status green] A global identifier used in finance; an active one is renewed yearly. checked 2026-10-15. GLEIF global LEI register (golden copy)
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. checked 2026-10-14. OpenSanctions
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. checked 2026-10-14. OpenSanctions
- Registered with the U.S. FDA (active, renewed for the current year) (record type: fda-registered) [official record; status green] Registered with the US food and drug regulator, renewed for the current year. checked 2026-10-14. FDA
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-10-14. Mail server of the company domain
- Takes part in public tenders (record type: public-contract-awarded) [official record; status green] 17 public contracts on record, the latest awarded 2025-10-07. A public buyer selected this supplier through an official tender. Open the source for the contracts themselves. effective since 2025-10-07. TED (Tenders Electronic Daily), EU public procurement award notices Tutaj wygrana niesie też cudzą kontrolę: w UE i EOG zamawiający musi wykluczyć wykonawcę skazanego za oszustwo, korupcję lub pranie pieniędzy oraz takiego, wobec którego prawomocnie stwierdzono zaległości podatkowe lub składkowe. Ta kontrola dotyczyła tamtego postępowania w dniu udzielenia zamówienia: nie pokazuje obecnej sytuacji firmy, a wygrana nie pokazuje, że umowa została wykonana. Directive 2014/24/EU, Article 57 (exclusion grounds)
- product-authorised-for-sale-holder (record type: product-authorised-for-sale-holder) [official record; status green] Applicant to the US FDA for 6 medical devices: Vivid E80 Diagnostic Ultrasound Imaging System, Vivid E90 Diagnostic Ultrasound Imaging System, Vivid E95 Diagnostic Ultrasound Imaging System (K150087, 2015-03-04), GE EchoPAC (K150085, 2015-03-02), 6VT-D ULTRASOUND TRANSDUCER (K141093, 2014-05-15) +3. The applicant answers for the notification; the record does not say who makes the device. A national regulator lists this company as the holder of the registration of products it has authorised for sale in that country. The holder answers for the product on that market; the record does not say the holder makes it. effective since 2026-10-05. FDA premarket notifications 510(k) and De Novo (openFDA, U.S. Food and Drug Administration)
- Legally registered and still active (record type: registry-active-global) [official record; status green] Shows the register lists the registration as active on the date we read it. It does not show how busy the business is. checked 2026-10-14. Brønnøysund (Enhetsregisteret)
- Line of business as recorded in the state register: Produksjon av strålingsutstyr, elektromedisinsk og elektroterapeutisk utstyr (record type: registry-activity) [official record; status green] Line of business as recorded in the state register: Produksjon av strålingsutstyr, elektromedisinsk og elektroterapeutisk utstyr. Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-10-14. Brønnøysund (Enhetsregisteret)
- Directors named in the company register (record type: leadership-on-record) [official record; status green] Registry lists Daglig leder: Dagfinn Sætre. The people leading the company are named in a public record. checked 2026-10-14. Brønnøysund (roller)
- Workforce size in the company register (record type: workforce-on-record) [official record; status green] 286 employees on the state record. One indication of the company's size as the register records it; it does not establish production capacity. checked 2026-10-14. Brønnøysund (antall ansatte)
- Registered business units on file (record type: registered-units) [official record; status green] 3 registered business units. The register lists how many sites the company runs. checked 2026-10-14. Brønnøysund (underenheter)
- Annual accounts filed with the register (record type: annual-accounts-filed) [official record; status green] Annual accounts filed for 2023, revenue NOK 1.7B. Indicates the company still meets its reporting duties. checked 2026-10-14. Regnskapsregisteret (Brønnøysund)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-10-17. ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-10-14. Domain registry record
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-10. GLEIF Global LEI record
- Owners named in the company register (record type: ownership-gleif-parent) [official record; status green] Ultimate accounting consolidating parent (GLEIF): GENERAL ELECTRIC COMPANY. GLEIF names the company's accounting consolidating parent: the entity that includes it in its consolidated financial statements. This is not a register of beneficial owners or of control. checked 2026-10-04. GLEIF global LEI index
Relationships
3 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Recorded in a source
- GENERAL ELECTRIC COMPANY: Consolidating parent (accounts), registry number 3C7474T6CDKPR9K6YT90. GLEIF global LEI index
Candidates, not confirmed
- gehealthcare.com: Website of this business. Source record
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)