Shockwave IVL System with the Shockwave M5 Peripheral IVL Catheter

FDA UDI

Class II (US FDA UDI)

by Shockwave Medical, Inc.

Identity

Trade Name: Shockwave IVL System with the Shockwave M5 Peripheral IVL Catheter FDA UDI
Generic Name: Ultrasound thrombolysis system catheter, peripheral FDA UDI
Device Name: 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). FDA UDI
Model / Reference: M5IVL6560 FDA UDI
Description: 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). FDA UDI

Identifiers

Catalog Number: M5IVL6560 FDA UDI
Primary DI / UDI-DI: M732M5IVL65600 FDA UDI
FDA Product Code: PPN FDA UDI
GMDN Term: Ultrasound thrombolysis system catheter, peripheral FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1250 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Working Length — 110 Centimeter FDA UDI
Balloon Length — 60 Millimeter FDA UDI
Balloon Rated Burst Pressure — 10 Atmosphere FDA UDI
Balloon Nominal (Inflation) Pressure — 6 Atmosphere FDA UDI
Guidewire Diameter — 0.014 Inch FDA UDI
Balloon Proximal Outer Diameter (OD) — 0.072 Inch FDA UDI
Introducer Sheath Compatibility — 7 French FDA UDI
Balloon Diameter — 6.5 Millimeter FDA UDI

Shockwave IVL System with the Shockwave M5 Peripheral IVL Catheter by Shockwave Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Shockwave Medical, Inc.

Sources (1)

FDA UDI 9ba8ab68-2d76-4c7e-9c59-88c54048e1e3 38 fields · synced May 30, 2026