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NanoCross™ Elite

FDA UDI

Class II (US FDA UDI)

by Ev3, Inc

Identity

Trade Name
NanoCross™ Elite FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name
PTA AB14W040020150 NANOCROSS 014 V05 FDA UDI
Model / Reference
AB14W040020150 FDA UDI
Description
PTA AB14W040020150 NANOCROSS 014 V05 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000110062 FDA UDI
510(k) Number
K141118 FDA UDI
FDA Product Code
DQY FDA UDI
LIT FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, basic 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 4.0 French FDA UDI
Length — 20.0 Millimeter FDA UDI
Outer Diameter — 4.0 Millimeter FDA UDI

Category: Peripheral angioplasty balloon catheter, basic

NanoCross™ Elite by Ev3, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ev3, Inc

Sources (1)

  • FDA UDI e10759cc-31d9-4d13-8bb6-a3c7cda7a8e8 37 fields · synced May 31, 2026