🚩 DEVICE: Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave M5+ (00195451000249)
Device Identifier (DI) Information
Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave M5+
5.5x60mm
In Commercial Distribution
M5PIVL5560
Shockwave Medical, Inc.
5.5x60mm
In Commercial Distribution
M5PIVL5560
Shockwave Medical, Inc.
The Shockwave M5+ Intravascular Lithotripsy (IVL) Catheter consists of an array of miniaturized lithotripsy emitters, located inside a balloon, that generate acoustic pressure waves within the target treatment site, disrupting calcium within the lesion and allowing subsequent dilation of a peripheral artery stenosis using low balloon pressure. Two radiopaque marker bands inside the balloon aid in positioning. The proximal hub has three ports: one for inflation/deflation of the balloon with 50/50 saline/contrast medium, one for the ‘Over-the-wire’ (OTW) guidewire lumen, and one for connection to the IVL Connector Cable (and IVL Generator).
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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66729 | Intravascular lithotripsy system balloon catheter, peripheral |
An electrically-powered, flexible tube intended to be introduced into a peripheral artery stiffened by a highly calcified atheromatous plaque, to transmit ultrasound (US) waves [e.g., acoustic pressure pulses] for the disruption of the plaque to improve vessel compliance. It is used in conjunction with a dedicated control unit/generator (not included) and includes transducers intended to convert electrical energy to ultrasound and an inflatable balloon at its distal end to facilitate energy transmission and dilation of the vessel. This is a single-use device.
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Active | false |
12535 | Medical equipment/instrument drape, single-use |
A flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment/instrument (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the equipment/instrument from soiling and/or contamination when used inside, or within the vicinity of, a hygienic area; it may have patient contact, however it is not intended to be introduced into a body cavity (noninvasive). It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
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OEZ | Cardiovascular Procedure Kit |
JAA | System, X-Ray, Fluoroscopic, Image-Intensified |
PPN | Percutaneous Catheter, Ultrasound |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Special Storage Condition, Specify: Keep dry and keep away from heat |
Clinically Relevant Size
[?]Size Type Text |
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Catheter Length: 135 Centimeter |
Balloon Diameter: 5.5 Millimeter |
Balloon Nominal (Inflation) Pressure: 6 Atmosphere |
Balloon Rated Burst Pressure: 10 Atmosphere |
Balloon Length: 60 Millimeter |
Introducer Sheath Compatibility: 6 French |
Balloon Proximal Outer Diameter (OD): 0.078 Inch |
Guidewire Diameter: 0.014 Inch |
Device Record Status
b21d92b2-ae82-48d9-9031-775756e6380f
September 11, 2024
6
May 11, 2021
September 11, 2024
6
May 11, 2021
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
1-877-775-4846
cs@shockwavemedical.com
cs@shockwavemedical.com