Model: ART-KW2-190
DI: 00841731138095
Status: New
MRI: Labeling does not contain MRI Safety Information
Single-use: Yes
Rx: Yes
OTC: No
First Published: 2026-05-15
Current Version: 2026-05-25
Description
ARTEMIS ZADEX K-WIRE, dia 2.2 X 190MM
Sterilization
Method Types - Sterilization Method:
Moist Heat or Steam Sterilization
Device Sterile:
No
Sterilization Prior To Use:
Yes
Regulatory & Distribution
Record Status:
Published
Version Number:
1
Record Key:
65f58a9e-bbae-49c8-80f7-2a63e3b2d4e0
Distribution Status:
In Commercial Distribution
DUNS Number:
117502293
Device Count:
1
DM Exempt:
No
Premarket Exempt:
No
HCT/P:
No
Kit:
No
Combination Product:
No
Lot/Batch Tracked:
Yes
Serial Number Tracked:
No
Manufacturing Date Tracked:
No
Expiration Date Tracked:
No
Donation ID Number Tracked:
No
Labeled Contains NRL:
No
Labeled No NRL:
No
Identifiers
Device ID:
00841731138095
Type:
Primary
Issuing Agency:
GS1
GMDN
Code: 62729
Name: Orthopaedic guidewire, single-use
Definition:
A thin, non-implantable rod designed to guide the insertion of a cannulated/tubular orthopaedic implant (typically an intramedullary nail, a bone screw or femoral fixation plate) and/or surgical instrument (e.g., drill bit) during an orthopaedic procedure. It is made of metal and is available in a variety of sizes, lengths, and designs (e.g., round-tip, trocar-tip, or flexible-tip). This is a single-use device.
FDA Product Codes
HXI
PASSER, WIRE, ORTHOPEDIC
Premarket Submissions
Submission Number:
K250304
Supplement Number:
000
Device Sizes
Device Size - Size Text:
N/A
Device Size - Size Type:
Device Size Text, specify
Environmental Conditions
Storage Handling - Storage Handling Type:
Special Storage Condition, Specify
Storage Handling - Storage Handling Special Condition Text:
N/A