LAERDAL MEDICAL AS
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Laerdal Medical - Contribuer à sauver des vies
Laerdal Medical est le premier fournisseur mondial de solutions de formation et de produits thérapeutiques liés au sauvetage et aux premiers secours.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Stavanger, Norway
- Founded
- 1997 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- https://laerdal.com
- Categories
- Fournitures médicales et de santé
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 14 official records from 11 official sources are on file. 5 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
- 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 2026-08-03. Mail server of the company domain
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 1999. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-03. Internet Archive (Wayback)
- 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 2026-08-03. OpenSanctions
- 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 2026-08-03. 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 2026-08-03. FDA
- Legally registered and still active (record type: registry-active-global) [official record; status green] Indicates the company is not dissolved or winding down. checked 2026-09-07. Norway Brønnøysund Register Centre (open bulk file)
- Active taxpayer registration (record type: tax-filing-active) [official record; status green] Registered as an active taxpayer. checked 2026-09-07. Norway Brønnøysund Register Centre (open bulk file)
- Workforce size in the company register (record type: workforce-on-record) [official record; status green] 631 employees on the state record. Tells you whether the supplier can realistically take on your volume. checked 2026-09-07. Norway Brønnøysund Register Centre (open bulk file)
- 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 2026-08-03. Domain registry record
- 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 2026-09-07. GLEIF global LEI register (golden copy)
- Places goods on the market (national producer register) (record type: places-goods-on-market; this record does not by itself establish manufacturing) [official record; status green] A state register lists this company as placing these goods on the market, as their maker or importer. By itself it does not show who makes them. checked 2026-09-07. Registre national des producteurs (ADEME/SYDEREP), France
- owns-trademark (record type: owns-trademark; this record does not by itself establish manufacturing) [official record; status green] Shows the company holds registered trademarks or patents in its own name. checked 2026-08-14. Norwegian Industrial Property Office (Patentstyret), IPR register
- Takes part in public tenders (record type: public-contract-awarded) [official record; status green] 4 public contracts on record, the latest awarded 2026-03-16. A public buyer selected this supplier through an official tender. Open the source for the contracts themselves. effective since 2026-03-16. TED (Tenders Electronic Daily), EU public procurement award notices Ici l'attribution porte aussi un contrôle fait par d'autres: dans l'UE et l'EEE, l'acheteur public doit exclure les candidats condamnés pour fraude, corruption ou blanchiment, ainsi que ceux dont une décision définitive a établi des dettes fiscales ou sociales. Ce contrôle valait pour cette procédure à la date de l'attribution: il ne montre pas la situation actuelle de l'entreprise, et une attribution ne montre pas que le marché a été exécuté. Directive 2014/24/EU, Article 57 (exclusion grounds)
- Annual accounts filed with the register (record type: annual-accounts-filed) [official record; status green] Annual accounts filed for 2023, revenue NOK 6.1B. Indicates the company still meets its reporting duties. checked 2026-10-02. Regnskapsregisteret (Brønnøysund)
- product-authorised-for-sale-holder (record type: product-authorised-for-sale-holder) [official record; status green] Applicant to the US FDA for 5 medical devices: The BAG manual resuscitator and accessories (K251631, 2025), NeoBeat, NeoBeat Mini (K232111, 2024), Reusable Silicone Cover CPRmeter 2 (K183348, 2018) +2. 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)
- Directors named in the company register (record type: leadership-on-record) [official record; status green] Registry lists Daglig leder: Alf Christian Dybdahl. The people leading the company are named in a public record. checked 2026-10-02. Brønnøysund (roller)
- Line of business as recorded in the state register: 32.500 (record type: registry-activity) [official record; status green] Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-09-07. Norway Brønnøysund Register Centre (open bulk file)
- 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. effective since 2026-07-11. Bronnoysund Register Centre, Central Coordinating Register of Legal Entities (Enhetsregisteret)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-10-03. ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
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)