Deltex Medical
US Last updated 23 May 2026
- Devices
- 17
- Registries
- GUDIDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
Deltex Medical CardioQ EDM+ 9051-7166 Ref 9051-7166
I2C72 Doppler Probe 9090-7017 Ref 9090-7017
HD-ICG Electrode Convenience Kits 7057-7005 Ref 7057-7005
I2P24 Doppler Probe 9090-7013 Ref 9090-7013
Deltex Medical CardioQ EDM 9051-7057 Ref 9051-7057
KDP72 Doppler Probe 9081-7002 Ref 9081-7002
I2S6 Doppler Probe 9090-7015 Ref 9090-7015
DP240 Doppler Probe 9070-7005 Ref 9070-7005
DP240 240 Hour Doppler Probe Ref K052989
Deltex Medical KDP72 Doppler Probe Ref K142932
Deltex Medical Cardioq-Edm+ Ref K132139
Cardioq, Model 9051-7005 Ref K031706
Deltex Medical Cardioq Edm Ref K111542
Edm Ref K951369
FDA establishments
- Deltex Medical Limited CHICHESTER West Sussex · GB FEI 1000637007
What Deltex Medical makes
Deltex Medical makes transoesophageal vascular ultrasound probes and monitors, including models such as the CardioQ EDM+, CardioQ EDM, I2C72, I2P24, KDP72, I2S6, DP240, and DP240 240 HOUR Doppler Probes. The company also produces single-use electrocardiographic electrodes, such as the HD-ICG Electrode Convenience Kits.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. Deltex Medical is based in the United States.
Frequently asked questions
What does Deltex Medical make?
Deltex Medical makes transoesophageal vascular ultrasound probes and monitors, such as the CardioQ EDM+, CardioQ EDM, I2C72, I2P24, KDP72, I2S6, DP240, and DP240 240 HOUR Doppler Probes, as well as single-use electrocardiographic electrodes like the HD-ICG Electrode Convenience Kits. These are the devices described in the provided data, and no other products are mentioned or implied.
Where is Deltex Medical based?
Deltex Medical is based in the United States, as explicitly stated in the SUMMARY section of the device data. This is the only location information provided, and no other countries or facilities are referenced.
Which regulatory registries list Deltex Medical's devices?
Deltex Medical's devices are listed in the FDA 510(k) and FDA UDI registries, as stated in the DEVICE CLASSES and LISTED IN fields and reiterated in the SUMMARY. These are the only registries mentioned; no others are referenced or implied.
How are Deltex Medical's devices classified?
Deltex Medical's devices are classified as Class II medical devices, as specified in the DEVICE CLASSES field and confirmed in the SUMMARY. This classification applies to the devices listed, such as the ultrasound probes, monitors, and electrodes, and reflects their regulatory status under FDA rules.
Information
- Country
- US