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Crosser®

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
CROSSER® FDA UDI
Generic Name
Mechanical atherectomy system catheter, coronary/peripheral FDA UDI
Device Name
CROSSER® CTO Recanalization Catheter 14S, Over the Wire, 106cm FDA UDI
Model / Reference
CRUOS106 FDA UDI
Description
CROSSER® CTO Recanalization Catheter 14S, Over the Wire, 106cm FDA UDI

Identifiers

Catalog Number
CRUOS106 FDA UDI
Primary DI / UDI-DI
10801741125611 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

Yes

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 — 106 Centimeter FDA UDI

Category: Mechanical atherectomy system catheter, coronary/peripheral

Crosser® 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 7ed7563b-9d87-4e91-923d-ed46fc41035a 36 fields · synced May 30, 2026