IEE Smart Sensing Solutions
Geavanceerde sensorsystemen voor de automobielsector, slimme gebouwen en de gezondheidszorg
IEE S.A. is een in Luxemburg gevestigde wereldwijde fabrikant van intelligente detectieoplossingen, met hoofdkantoor in Bissen. Het bedrijf produceert geavanceerde sensoren voor de detectie van inzittenden voor de veiligheid van auto's, sensoren voor het tellen van mensen en toegangscontrole voor slimme gebouwen, en medische bewakingsapparatuur. IEE-sensoren zijn wereldwijd in honderden miljoenen voertuigen geïntegreerd.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Bissen, Luxembourg
- Founded
- 1989
- Website
- iee-sensing.com
- Categories
- Consumentenelektronica, Smart Home & IoT, Medische en gezondheidszorgbenodigdheden
- Markets
- Duitsland, Frankrijk, Verenigd Koninkrijk, Verenigde Staten, 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
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-08 Domain registry record
- vat-valid (green), checked 2026-08-08 VIES
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management 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)
- 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)