IN-DATE
RC1414025: IMDS Recross OTW Dual Lumen Guidewire Support Catheter 140cm
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| Price: | $349.00 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 10 box of 1 |
| Status: | expired |
Additional Details
IMDS Recross OTW Dual Lumen Guidewire Support Catheter
The ReCross is a dual lumen catheter intended to use in the coronary and/or peripheral vasculature. The ReCross is a 0.014” Over The Wire (OTW) guide wire support catheter. The ReCross has two over the wire OTW lumens that runs the length of the catheter. The ReCross has two depth markings located at 95 cm and 105 cm from the distal tip. The ReCross has a radiopaque marker identifying the distal end of the catheter, a second radiopaque marker in the stylet lumen located 8 mm from the distal tip identifies the distal end of the OTW lumen and a third radiopaque marker in the tip lumen located at 12 mm from the distal tip indentifying the side port. To reduce friction in the guide catheter and vasculature, the distal shaft is fitted with a hydrophilic coating. To reduce friction of the guide wire in the lumen, the entire lumens of the ReCross are coated with MDX (silicone) coating. To ease catheter loading into the hemostasis device and the guiding catheter a removable stylet is placed in the stylet lumen
Product Code: RC1414025
- 0.014" Over-The-Wire (OTW)
- 140cm
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use
- Disposable
Additional Details
- Company Name: IMDS Operations B.V.
- FDA Product Code: DQY
- FDA Product Code Name: Catheter, Percutaneous
- GMDN Term Code: 17846
- GMDN Term Name: Vascular guide-catheter, single-use
- GMDN Term Definition: A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.
AccessGUDID Info
- FDA Product Code: DQY
- FDA Product Code Name: Catheter, Percutaneous
- GMDN Term Code: 17846
- GMDN Term Name: Vascular guide-catheter, single-use
- GMDN Term Description: A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.
Manufacturer
IMDS (Innovative Mechanical Design Services) is a Netherlands-based medical device company specializing in the design and manufacturing of minimally invasive spinal implants and delivery systems. With a focus on interventional spine procedures, IMDS develops innovative, single-use devices that support targeted therapies for conditions such as vertebral compression fractures, spinal tumors, and disc degeneration. Its portfolio includes vertebral body augmentation systems, steerable needles, and implantable spacers engineered for precise navigation and controlled deployment. IMDS serves as both a product innovator and OEM partner, offering design, development, and contract manufacturing services to leading medtech companies worldwide.
