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VSI Guidewire

FDA UDI

Class II (US FDA UDI)

by Vascular Solutions, Inc.

Identity

Trade Name
VSI Guidewire FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
Guidewires are intended for use in percutaneous procedures to introduce and position catheters and other interventional devices within the coronary, and peripheral vasculature. FDA UDI
Model / Reference
7343 FDA UDI
Description
Guidewires are intended for use in percutaneous procedures to introduce and position catheters and other interventional devices within the coronary, and peripheral vasculature. FDA UDI

Identifiers

Primary DI / UDI-DI
M20673430 FDA UDI
FDA Product Code
DQX FDA UDI
GMDN Term
Peripheral vascular guidewire, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.014 Inch FDA UDI
Length — 50 Centimeter FDA UDI

Category: Peripheral vascular guidewire, manual

VSI Guidewire by Vascular Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular guidewire, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vascular Solutions, Inc.

Sources (1)

  • FDA UDI 59c048b5-93b5-4ba7-abc2-2df9eb58d401 35 fields · synced Jun 1, 2026