IDEXX Laboratories
التشخيص البيطري والتحليلات ومنتجات اختبار صحة الحيوان.
تقوم مختبرات IDEXX بتصنيع أدوات التشخيص البيطرية والمحللات ومنتجات اختبار صحة الحيوان من عمليات Westbrook التابعة لها. توفر الشركة أنظمة الرعاية الصحية والمختبرات وشركاء تصنيع المعدات الأصلية أو عملاء التصدير الخاضعين للتنظيم عبر أسواقها الرئيسية المدرجة.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Westbrook, United States
- Founded
- 1983
- Website
- idexx.com
- Categories
- اللوازم الطبية والرعاية الصحية, رعاية الحيوانات الأليفة وملحقاتها
- Markets
- الولايات المتحدة, ألمانيا, اليابان, أستراليا
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
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- facility-registered (green), effective since 2026-08-07 US EPA Facility Registry Service (national combined file)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- industrial-permit (green), checked 2026-08-23 ECHO, Enforcement and Compliance History Online (U.S. Environmental Protection Agency)
- 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
- ISO 9001, Quality Management IAF CertSearch
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)
- Consumer goods sold in the EU fall under the General Product Safety Regulation (GPSR, applies since 13 Dec 2024): a responsible person in the EU is mandatory. EUR-Lex: Regulation (EU) 2023/988 (GPSR)