Demant
Medische apparaten, gezondheidszorgbenodigdheden en klinische producten.
Demant produceert medische apparatuur, gezondheidszorgbenodigdheden en klinische producten vanuit zijn Smorum-activiteiten. Het bedrijf levert aan ziekenhuiskopers, klinische distributeurs, gezondheidszorgsystemen en exportklanten op zijn beursgenoteerde primaire markten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Smorum, Denmark
- Founded
- 1904
- Website
- demant.com
- Categories
- Medische en gezondheidszorgbenodigdheden, Industriële benodigdheden
- Markets
- Denemarken, Verenigde Staten, Duitsland, Japan
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
- annual-accounts-filed (green), checked 2026-08-16 Erhvervsstyrelsen, offentliggjorte årsrapporter (virk.dk)
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
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)