Home GUDID 00886385011608 RINGFIX
Primary DI 00886385011608
Brand RINGFIX
Company Stryker Trauma SA
Model 955-1023
Catalog number 955-1023
Device description Shoulder Bolt
Published 2016-09-24
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 00886385011608 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 00886385011608 00886385011608 886385011608 0886385011608
GMDN Terms# Term, Definition table Term Definition External orthopaedic fixation system, single-use, non-sterile An assembly of non-sterile devices designed to stabilize fractured bones to promote treatment and healing. It typically consists of an external plastic and/or metallic fixator (a framework) and other external and/or implantable components such as clamps, rods, rings, pins, bolts, and nuts, as well as some reusable instrumentation (e.g., wrenches, depth gauge, tensioner). It is used mainly to help the healing of long bones such as the femur, tibia and humerus, as well as fractures of the foot and ankle, joint fusions, and limb lengthening. This is a single-use device intended to be sterilized prior to use.
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