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PressureWire™

FDA UDI

Class II (US FDA UDI)

by Lightlab Imaging, Inc.

Identity

Trade Name
PressureWire™ FDA UDI
Generic Name
Cardiac/peripheral vascular guidewire, single-use FDA UDI
Device Name
X Guidewire FDA UDI
Model / Reference
C12359 FDA UDI
Description
X Guidewire FDA UDI

Identifiers

Catalog Number
C12359 FDA UDI
Primary DI / UDI-DI
05415067025722 FDA UDI
FDA Product Code
DXO FDA UDI
DRG FDA UDI
DQX FDA UDI
GMDN Term
Cardiac/peripheral vascular guidewire, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2870 FDA UDI
870.2910 FDA UDI
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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.014 Inch FDA UDI
Length — 300 Centimeter FDA UDI

Category: Cardiac/peripheral vascular guidewire, single-useCatheter-tip transducer, pressure

PressureWire™ by Lightlab Imaging, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catheter-tip transducer, pressure.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55b1ea26-6fc7-48ba-98ae-1cb0d78f170b 37 fields · synced May 30, 2026