Beurer GmbH
الشركة المصنعة الألمانية للصحة والعافية والأجهزة المتصلة.
تقوم شركة Beurer بتصنيع أجهزة مراقبة ضغط الدم ومقاييس الحرارة والمقاييس وأجهزة التدليك والأجهزة القابلة للارتداء والإلكترونيات الصحية. تأسست الشركة في ألمانيا عام 1919، وتقوم بتزويد الصيدليات وتجار الإلكترونيات بالتجزئة وموزعي الرعاية الصحية في جميع أنحاء العالم.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ulm, Germany
- Founded
- 1919
- Website
- beurer.com
- Categories
- الأجهزة القابلة للارتداء والأجهزة الشخصية, اللوازم الطبية والرعاية الصحية
- Markets
- ألمانيا, النمسا, فرنسا, المملكة المتحدة
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)