Agilent Technologies
Instrumen analitik, diagnostik, reagen, dan bahan habis pakai laboratorium.
Agilent Technologies memproduksi instrumen analitik, diagnostik, reagen, dan bahan habis pakai laboratorium dari operasinya di Santa Clara. Perusahaan ini memasok sistem perawatan kesehatan, laboratorium, mitra OEM, atau pelanggan ekspor teregulasi di seluruh pasar utama terdaftarnya.
- Type
- Manufacturer
- Location
- Santa Clara, United States
- Founded
- 1999
- Website
- agilent.com
- Categories
- Perlengkapan Medis & Kesehatan, Mesin Industri
- Markets
- Amerika Serikat, Jerman, Jepang, Tiongkok
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