Agilent Technologies
Instrumentos analíticos, diagnósticos, reactivos y consumibles de laboratorio.
Agilent Technologies fabrica instrumentos analíticos, diagnósticos, reactivos y consumibles de laboratorio en sus operaciones de Santa Clara. La empresa suministra sistemas de atención médica, laboratorios, socios OEM o clientes de exportación regulados en sus mercados primarios listados.
- Type
- Manufacturer
- Location
- Santa Clara, United States
- Founded
- 1999
- Website
- agilent.com
- Categories
- Suministros médicos y sanitarios, Maquinaria industrial
- Markets
- Estados Unidos, Alemania, Japón, China
Verified facts
- domain-registered (green), checked 2026-08-12 Domain registry record
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- fda-registered (green), checked 2026-08-12 FDA
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- 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)
- facility-registered (green), checked 2026-08-03 US EPA Facility Registry Service
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 9001, Quality Management IAF CertSearch
- FDA Registered FDA Establishment Registration
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission