Agilent Technologies
विश्लेषणात्मक उपकरण, निदान, अभिकर्मक और प्रयोगशाला उपभोग्य वस्तुएं।
एगिलेंट टेक्नोलॉजीज अपने सांता क्लारा परिचालन से विश्लेषणात्मक उपकरण, निदान, अभिकर्मकों और प्रयोगशाला उपभोग्य सामग्रियों का निर्माण करती है। कंपनी अपने सूचीबद्ध प्राथमिक बाजारों में स्वास्थ्य देखभाल प्रणालियों, प्रयोगशालाओं, ओईएम भागीदारों या विनियमित निर्यात ग्राहकों को आपूर्ति करती है।
- Type
- Manufacturer
- Location
- Santa Clara, United States
- Founded
- 1999
- Website
- agilent.com
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, औद्योगिक मशीनरी
- Markets
- संयुक्त राज्य, जर्मनी, जापान, चीन
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