← Back to catalogue

Xwire

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
XWIRE FDA UDI
Generic Name
Gastro-urological guidewire, single-use FDA UDI
Device Name
XWire® Biliary Guidewire 450 cm Angled Tip, .64 mm Guidewire Length, Standard Wire, .025" O.D. FDA UDI
Model / Reference
025450A FDA UDI
Description
XWire® Biliary Guidewire 450 cm Angled Tip, .64 mm Guidewire Length, Standard Wire, .025" O.D. FDA UDI

Identifiers

Catalog Number
025450A FDA UDI
Primary DI / UDI-DI
20653405053986 FDA UDI
510(k) Number
K011759 FDA UDI
FDA Product Code
OCY FDA UDI
GMDN Term
Gastro-urological guidewire, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 450 Centimeter FDA UDI
Outer Diameter — 0.025 Inch FDA UDI
Outer Diameter — 0.64 Millimeter FDA UDI

Category: Gastro-urological guidewire, single-use

Xwire by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological guidewire, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 109006e7-72c7-444a-8eba-7369ad9165a8 37 fields · synced May 30, 2026