Honeywell, Inc.
United StatesFDA applicant, unverified
- Devices
- 69
What Honeywell, Inc. makes
Honeywell, Inc. manufactures portable and bedside cardiac monitoring devices, including defibrillators (e.g., ED 425, 74DRK), patient monitors (e.g., CM111, CM112), and ECG monitors (e.g., RM102). The company also produces diagnostic imaging tools like the ULTRA IMAGER and motility assessment equipment such as the esophageal motility apparatus. Additional offerings include electrophysiological recording systems (e.g., AR110, N3B-EEG amplifier), pulse/phonocardiography channels, and medical data management solutions for reporting and database tracking.
The company’s devices are classified under FDA categories Class I, Class II, and Class III, with submissions recorded in the FDA’s 510(k) registry. These products are listed under U.S. regulatory oversight, reflecting compliance with U.S. medical device requirements. The manufacturer operates from the United States.
Catalogue
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