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VSI Tru-Torque™ guidewire

FDA UDI

Class II (US FDA UDI)

by Vascular Solutions, Inc.

Identity

Trade Name
VSI Tru-Torque™ guidewire FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
The VSI Tru-Torque Steerable Guidewire facilitates placement of a catheter during diagnostic angiography and interventional procedures. The VSI Tru-Torque can be accurately controlled ot facilitate navigation through tortuous vessels and/or adjoining side branches. FDA UDI
Model / Reference
7471 FDA UDI
Description
The VSI Tru-Torque Steerable Guidewire facilitates placement of a catheter during diagnostic angiography and interventional procedures. The VSI Tru-Torque can be accurately controlled ot facilitate navigation through tortuous vessels and/or adjoining side branches. FDA UDI

Identifiers

Primary DI / UDI-DI
M20674710 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
Not 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.035 Inch FDA UDI
Length — 300 Centimeter FDA UDI

VSI Tru-Torque™ guidewire by Vascular Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 713ab9a5-5614-4171-9563-37a9ea569262 36 fields · synced May 31, 2026