Contract manufacturerCARDIONET, LLC (Phoenix, AZ)ArizonaCardiovascularPhysical medicineClass II
CARDIONET, LLC
Contract manufacturer ยท Phoenix, AZ
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3008773647 (openFDA record; or search FDA's registration database)
- FEI number
- 3008773647
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Contract manufacturer
- Owner or operator
- Philips Medical Systems International BV (FDA owner/operator no. 1217116)
- Registered address
- 5750 S. 40th St Suite 5, Phoenix, AZ 85040
- Contract listings
- 4 device listings, 4 product codes, first listed Nov 12, 2003
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| DRX | Electrode, Electrocardiograph | Class II | Cardiovascular | Contract manufacturing | Feb 23, 2022 |
| DSH | Recorder, Magnetic Tape, Medical | Class II | Cardiovascular | Contract manufacturing | Nov 6, 2023 |
| DSI | Detector And Alarm, Arrhythmia | Class II | Cardiovascular | Contract manufacturing | Nov 6, 2023 |
| IKD | Cable, Electrode | Class II | Physical medicine | Contract manufacturing | Nov 12, 2003 |