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Wholey™

FDA UDI

Class II (US FDA UDI)

by Ev3, Inc

Identity

Trade Name
Wholey™ FDA UDI
Generic Name
Peripheral vascular guidewire extension FDA UDI
Device Name
GW WWES35001 WHOLEY WIRE EXT SYSTEM NCE FDA UDI
Model / Reference
WWES35001 FDA UDI
Description
GW WWES35001 WHOLEY WIRE EXT SYSTEM NCE FDA UDI

Identifiers

Primary DI / UDI-DI
00763000919634 FDA UDI
510(k) Number
K120863 FDA UDI
FDA Product Code
DQX FDA UDI
GMDN Term
Peripheral vascular guidewire extension 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Guidewire Diameter — 0.089 Centimeter FDA UDI
Guidewire Length — 155.0 Centimeter FDA UDI

Category: Peripheral vascular guidewire extension

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

Similar devices

Also classified as Peripheral vascular guidewire extension.

Cleared under the same submission

K120863 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ev3, Inc

Sources (1)

  • FDA UDI 8fe7f0df-8ec9-47ab-b1ea-fd9076de2331 37 fields · synced Jun 8, 2026