Home GUDID 00886385010182 RINGFIX
Primary DI 00886385010182
Brand RINGFIX
Company Stryker Trauma SA
Model 451-2005
Catalog number 451-2005
Device description K-Wire, DLC
Published 2015-09-24
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00886385010182 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00886385010182 00886385010182 886385010182 0886385010182
GMDN Terms# Term, Definition table Term Definition Fluted surgical drill bit, reusable A shaft of metal with an obtuse, V-shaped cutting edge designed to be rotated to bore into bone to create a hole of the same dimension as the diameter of the shaft. This device, commonly called a "twist drill", has a cylindrical design with a double-edged cutting head that is formed from two spiralled flutes that extend the length of the insertion part of the drill. At the proximal end, it is usually inserted into a surgical power tool or a surgical hand drill/brace. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 400 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 481999654 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00888867516465 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867516472 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867518681 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543157 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543256 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543331 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543348 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543355 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543362 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543379 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543386 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543393 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543409 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543478 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543591 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543607 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543638 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543645 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543676 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543690 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543706 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543713 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543799 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543843 Arthrex® ARTHREX, INC. KTT 2026-03-13 00888867543881 Arthrex® ARTHREX, INC. KTT 2026-03-13 00841731149077 DYNEX MICRO VILEX LLC KTT 2026-03-03 00889795151827 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16 00889795151834 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16 00889795151841 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16 00889795151858 The Brachiator Mini External Fixation System Paragon 28, Inc. KTT 2025-12-16