CATH CEDT200L UNIDIR LG CURVE US
DiamondTemp™ Unidirectional Ablation Catheter - CEDT200L
Device Description
A sterile, flexible, steerable catheter intended to be used as part of a radio-frequency cardiac ablation system to apply radio-frequency alternating current to ablate areas of the endocardium of a beating heart in the treatment of cardiac arrhythmias; it is typically also intended to transmit electrical pacing stimuli to, and electrical responses from, the heart for electrophysiological (EP) mapping. It is intended to be introduced into the heart via venous access (e.g., femoral vein) and may contain monopolar and/or bipolar ablation electrodes. This is a single-use device.
Environmental Conditions
- 140.00
- -22.00
- Keep away from sunlight
- Keep dry
- 86.00
- 59.00
Device Sizes
- Catheter Length: 110.0 Centimeter
- Catheter tip size 2.50mm (7.5Fr)
- Electrode spacing between distal electrode and proximal electrode .5mm
- Electrode spacing between composite electrode and distal ring electrode 3.5mm
- Ring electrode length 1.3mm
- Electrode spacing between distal ring electrode and proximal ring electrode 2mm
- Composite tip electrode length 4.1mm
- Distal electrode length .6mm
- Tip Bend Radius: 63.0 Millimeter
- Outer Diameter: 2.67 Millimeter
Device Sterilization
Device Sterile: True
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: OAE
Device Name: Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
Device Class: 3
Physical State: The device is an ablation catheter that features electrodes through which thermal energy is delivered.
Definition: For the treatment of atrial fibrillation.
Submission Type ID: 2
Review Panel: CV
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: The ablation catheter delivers energy to the specific region of the heart in order to create lesions that will treat the patient of atrial fibrillation.
Life Sustain Support Flag: Y
Unclassified Reason: N/A
Implant Flag: N
Target Area: Heart
Regulation Number: N/A
Third Party Flag: N
Medical Specialty: N/A
Device IdentifiersDevice Id: 00763000482114
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A