Design Features
- Single lumen, torqueable Imager catheter are available in five tip configurations and 3 working lengths
- Biocompatible polymer reinforced with a stainless steel braided wire
- Luer lock hub attached at the proximal end
Multiple Sizes
- Offered in 5 Open Tip configuration
- 5F diameter with 3 working lengths
Placement
- Facilitates access to the urinary tract with various tip designs
- Can be placed either retrograde or antegrade
- Excellent radiopacity for improved visualization
Latex Information
This product contains no detectable latex.
MVO1170
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Ordering Information
| Order Number | Description | O.D. Size | Working Length(cm) | Quantity |
|---|---|---|---|---|
| M0064003001 | C1 | 5F | 65 | Box 5 |
| M0064003011 | C2 | 5F | 65 | Box 5 |
| M0064003021 | Straight | 5F | 65 | Box 5 |
| M0064003031 | Bern | 5F | 65 | Box 5 |
| M0064003041 | JB1 | 5F | 65 | Box 5 |
| M0064004021 | Straight | 5F | 100 | Box 5 |
| M0064004031 | Bern | 5F | 100 | Box 5 |
| M0064004041 | JB1 | 5F | 100 | Box 5 |
| M0064005031 | Bern | 5F | 40 | Box 5 |
Prescriptive Information
Prescriptive Information
Refer to the operator's manual for complete instructions for use.
Contraindications
This device is, in general, contraindicated for use in patients who are unsuitable for ureteral catheterization or the infusion of contrast material.
Warnings
Contents supplied STERILE using an ethylene oxide (EO) process. Do not use if sterile barrier is damaged. If damage is found call your Boston Scientific representative. For single patient use only. Do not reuse, reprocess or resterilize. Reuse, reprocessing or resterilization may compromise the structural integrity of the device and/or lead to device failure which, in turn, may result in patient injury, illness or death. Reuse, reprocessing or resterilization may also create a risk of contamination of the device and/or cause patient infection or cross-infection, including, but not limited to, the transmission of infectious disease(s) from one patient to another. Contamination of the device may lead to injury, illness or death of the patient. After use, dispose of product and packaging in accordance with hospital, administrative and/or local government policy.
Potential Adverse Effects
The complications which may result from ureteral catheter placement include, but are not limited to:
- Extravasation
- Hemorrhage
- Sepsis
- Edema
- Loss of Renal Function
- Perforation of kidney, renal pelvis, ureter and bladder
- Peritonitis
- Urinary tract infection
Cautions
- Avoid bending or kinking the catheter prior to placement. To do so could damage the integrity of the catheter and result in patient injury.
- If resistance is encountered during advancement or withdrawal of the catheter, STOP. DO NOT CONTINUE without first determining the cause of the resistance and taking remedial action.
Indications
The Imager II Urology Torque Catheter is indicated for use in facilitating access to the urinary tract, either through a retrograde or antegrade route, and may be used in conjunction with a guidewire or for the infusion of radiopaque contrast material.
Federal (USA) law and governing law outside the USA restrict these devices to sale by or on the order of a physician.
Product Callouts
Reimbursement
Supporting Materials