Beurer GmbH
Duitse fabrikant van gezondheids-, welzijns- en verbonden apparaten.
Beurer produceert bloeddrukmeters, thermometers, weegschalen, massageapparaten, wearables en wellness-elektronica. Het bedrijf werd in 1919 in Duitsland opgericht en levert wereldwijd aan apotheken, elektronicaretailers en gezondheidszorgdistributeurs.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ulm, Germany
- Founded
- 1919
- Website
- beurer.com
- Categories
- Wearables en persoonlijke apparaten, Medische en gezondheidszorgbenodigdheden
- Markets
- Duitsland, Oostenrijk, Frankrijk, Verenigd Koninkrijk
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
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- domain-registered (green), checked 2026-08-02 Domain registry record
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- energy-market-role (green), checked 2026-08-17 Marktstammdatenregister (Bundesnetzagentur)
- vat-valid (green), checked 2026-08-13 VIES (European Commission)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI 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)
- 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)