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Crosser iQ

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
Crosser iQ FDA UDI
Generic Name
Mechanical atherectomy system catheter, coronary/peripheral FDA UDI
Device Name
Crosser iQ Ultrasonic CTO Device FDA UDI
Model / Reference
XCTO146 FDA UDI
Description
Crosser iQ Ultrasonic CTO Device FDA UDI

Identifiers

Catalog Number
XCTO146 FDA UDI
Primary DI / UDI-DI
00801741201332 FDA UDI
FDA Product Code
PDU FDA UDI
GMDN Term
Mechanical atherectomy system catheter, coronary/peripheral FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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
Length — 146 Centimeter FDA UDI

Category: Mechanical atherectomy system catheter, coronary/peripheral

Crosser iQ by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical atherectomy system catheter, coronary/peripheral.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Peripheral Vascular

Sources (1)

  • FDA UDI ee147d27-b0e9-485c-b5f8-784d03dafaa9 36 fields · synced May 30, 2026