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Agilent Technologies, Inc.

United States·US-MF-000009385

Last updated September 17, 2026

Information

Country
United States
Address
5301, Stevens Creek Blvd., Santa Clara, United States
LinkedIn
—
Facebook
—
Phone
+45 44859756
PRRC Contact
Grace Lee
EUDAMED SRN
US-MF-000009385
FDA FEI Number
1217454
DUNS Number
—

Catalogue (69)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Artisan Masson's Trichrome Stain Kit AR173
EUDAMED
Class AActive
Artisan Jones' Basement Membrane Stain Kit AR180
EUDAMED
Class AActive
Artisan PAS-Green Stain Kit AR172
EUDAMED
Class AActive
Dako EnVision+ System- HRP Labelled Polymer Anti-mouse K4001
EUDAMED
Class AActive
Artisan Iron Stain Kit AR158
EUDAMED
Class AActive
Artisan Elastic Stain Kit AR163
EUDAMED
Class AActive
Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A K5899
EUDAMED
Class AActive
Dako Antibody Diluent S0809
EUDAMED
Class AActive
Artisan Gram Yellow Stain Kit AR306
EUDAMED
Class AActive
Artisan Grocott's Methenamine Silver Stain Kit AR176
EUDAMED
Class AActive
Dako DAB Enhancer S1961
EUDAMED
Class AActive
Envision FLEX DAB Enhancer (Dako Omnis) GC806
EUDAMED
Class AActive
Instrument Cleaning Kit For Automated Link Platforms SK301
EUDAMED
Class AActive
Artisan Mucicarmine Stain Kit AR168
EUDAMED
Class AActive
Artisan Masson's Trichrome Stain Kit AR173
EUDAMED
Class AActive
ISH Cleaning Solution (Dako Omnis) GC207
EUDAMED
Class AActive
Protein Block Serum-Free Ready-to-Use X0909
EUDAMED
Class AActive
Dako Antibody Diluent with Background Reducing Components S3022
EUDAMED
Class AActive
Artisan Artisan Clearing Solution AR309
EUDAMED
Class AActive
Epoch Epoch-SI
EUDAMEDFDA UDI
Class AActive
Ari Standard Anesthesia Record K854213
FDA 510(k)
Class IIActive
Hp M2376a Device Link System, Model M2376a K002009
FDA 510(k)
Class IIActive
M2410b Imagepoint Hx Multispecialty System, Version B.1 K001711
FDA 510(k)
Class IIActive
Viridia Information Center Software For M3150a And M3153a, Viridia Telemetry System Transmitter K000854
FDA 510(k)
Class IIActive
Modification To Hp M2376a Device Link System K000635
FDA 510(k)
Class IIActive
Pagewriter 10/10i, Model M2662a Handheld Electrocardiograph K002459
FDA 510(k)
Class IIActive
Agilent M2636a Telemon Monitor K001436
FDA 510(k)
Class IIActive
Compact Portable Patient Monitor With Wireless Alan, Model Alilent M3000a/M3046a Option J120 K001664
FDA 510(k)
Class IIActive
Heartstream Fr2 Aed, Model M3860a, M3861a K003565
FDA 510(k)
Class IIIActive
M2376a Devicelink System, Model M2376a K002967
FDA 510(k)
Class IIActive
M2430 Diagnostic Ultrasound System With The 21420 Transducer K002397
FDA 510(k)
Class IIActive
Heartstream Xl Defibrillator/Monitor, Model M4735a K001725
FDA 510(k)
Class IIIActive
Agilent Information Center Software For M3150, M3151, M3153 And M3154 K011093
FDA 510(k)
Class IIActive
GenetiSure Dx Postnatal Assay K163367
EUDAMEDFDA 510(k)FDA UDI
Class IIActive
M2376a Devicelink System K003107
FDA 510(k)
Class IIActive
M2376a Devicelink System K010048
FDA 510(k)
Class IIActive
M2376a Devicelink System, Model M2376a K003622
FDA 510(k)
Class IIActive
Modification To Device Link System, Model M2376a K012094
FDA 510(k)
Class IIActive
Heartstream Attenuated Defibrillation Pads, Model M3870a K003819
FDA 510(k)
Class IIIActive
M2376a Devicelink System, Model M2376a K010342
FDA 510(k)
Class IIActive
M2424a Sonos 5500/4500 Diagnostic Ultrasound System, Version B.2. 21330a Transducer K002470
FDA 510(k)
Class IIActive
M2376a Devicelink System, Model M2376a K011578
FDA 510(k)
Class IIActive
St/Ar St And Arrhythmia Software K001348
FDA 510(k)
Class IIActive
Heartstream Xl Defibibrillator/Monitor, Model M4735a, Heartstream Xlt Defibrillator/Monitor.model M2500b K010634
FDA 510(k)
Class IIIActive
Agilent M2636b Telemon B Monitor (telemon B) K011824
FDA 510(k)
Class IIActive
Modification To Hp M2376a Device Link System, Model M2376a K001776
FDA 510(k)
Class IIActive
Viridia Information Center Software For M3154a Opt C22 K993907
FDA 510(k)
Class IIActive
M2376a Devicelink System K010453
FDA 510(k)
Class IIActive
St/Ar St And Arrhythmia Software, Model Release D.0 K003621
FDA 510(k)
Class IIActive
Agilent Information Center Software For M3150a And M3153a And Agilent M2/M3/M4 Compact Portable Patient Monitor K001057
FDA 510(k)
Class IIActive

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