Home GUDID 00889024489660
Trabecular Metal Reverse Plus™
Primary DI 00889024489660
Brand Trabecular Metal Reverse Plus™
Company Zimmer, Inc.
Model 00-4361-043-00
Catalog number 00-4361-043-00
Published 2019-06-07
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Product Codes# Code, Name table Code Name HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED PHX shoulder prosthesis, reverse configuration
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented Orthopedic 2 KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented Orthopedic 2 KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented Orthopedic 2 PHX Shoulder Prosthesis, Reverse Configuration Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00889024489660 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 00889024489660 00889024489660 889024489660 0889024489660
GMDN Terms# Term, Definition table Term Definition Surgical drill guide, reusable A hand-held tubular surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone), and to protect the surrounding soft tissue while the drill is in operation. It may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle at its proximal end for holding and manipulation, or it may be held by another device (e.g., orthopaedic jig). The device is typically dedicated to drill bit size, made of metal, and may have graduations along its length; it is not custom-made for a specific patient. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 056038268 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00889024701670 Identity® Shoulder System 120004657 120004657 2026-06-09 00889024707382 Persona Tensor Sizer Arm – Long SSI008513 SSI008513 2026-05-29 00889024707399 Persona Tensor Sizer Arm – Std SSI008567 SSI008567 2026-05-29 00889024707405 Persona Tensor Sizer Body SSI008566 SSI008566 2026-05-29 00889024081024 XtraFix® Large External Fixation System 00-5207-024-30 00-5207-024-30 2016-08-09 00889024081055 XtraFix® Large External Fixation System 00-5207-032-30 00-5207-032-30 2016-07-27 00889024081062 XtraFix® Large External Fixation System 00-5207-040-10 00-5207-040-10 2016-07-28 00889024081079 XtraFix® Large External Fixation System 00-5207-040-70 00-5207-040-70 2016-07-28 00889024081086 XtraFix® Large External Fixation System 00-5207-045-10 00-5207-045-10 2016-07-28 00889024081093 XtraFix® Large External Fixation System 00-5210-009-01 00-5210-009-01 2016-09-28 00889024081109 XtraFix® Large External Fixation System 00-5210-009-02 00-5210-009-02 2016-09-28 00889024081147 XtraFix® Large External Fixation System 00-5210-019-01 00-5210-019-01 2016-09-28 00889024081154 XtraFix® Large External Fixation System 00-5210-029-01 00-5210-029-01 2016-09-28 00889024081178 XtraFix® Large External Fixation System 00-5210-040-00 00-5210-040-00 2016-09-28 00889024081185 XtraFix® Large External Fixation System 00-5210-040-01 00-5210-040-01 2016-09-28 00889024081192 XtraFix® Large External Fixation System 00-5210-040-02 00-5210-040-02 2016-09-28 00889024081208 XtraFix® Large External Fixation System 00-5210-040-03 00-5210-040-03 2016-09-28 00889024081215 XtraFix® Large External Fixation System 00-5210-040-04 00-5210-040-04 2016-09-28 00889024081239 XtraFix® Large External Fixation System 00-5210-040-06 00-5210-040-06 2016-09-28 00889024081253 XtraFix® Large External Fixation System 00-5210-050-01 00-5210-050-01 2016-09-28
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840097535678 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535692 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535715 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535739 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535753 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535777 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535791 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535814 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535838 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535852 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535876 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097535890 Veritas rTSA Restor3d, Inc. PHX 2026-06-03 00840097534978 Veritas rTSA Restor3d, Inc. PHX 2026-06-02 00840097534985 Veritas rTSA Restor3d, Inc. PHX 2026-06-02 B1132A2HI000100 Shoulder Innovations InSet 95 Humeral Stem Shoulder Innovations, Inc. KWS 2026-05-28 B1132A2HI000100 Shoulder Innovations InSet 95 Humeral Stem Shoulder Innovations, Inc. KWT 2026-05-28 B1132A2HI000100 Shoulder Innovations InSet 95 Humeral Stem Shoulder Innovations, Inc. HSD 2026-05-28 07613327354331 REUNION Stryker GmbH KWS 2022-11-15 07613327354355 REUNION Stryker GmbH KWS 2022-11-15 07613327354379 REUNION Stryker GmbH HSD 2022-11-15 07613327354386 REUNION Stryker GmbH HSD 2022-11-15 07613327354799 REUNION Stryker GmbH HSD 2022-11-15 07613327354805 REUNION Stryker GmbH KWS 2022-11-15 07613327354324 REUNION Stryker GmbH HSD 2022-11-14 07613327354317 REUNION Stryker GmbH HSD 2021-04-27 07613327354317 REUNION Stryker GmbH PHX 2021-04-27 07613327354348 REUNION Stryker GmbH HSD 2021-04-27 07613327354348 REUNION Stryker GmbH PHX 2021-04-27 07613327354362 REUNION Stryker GmbH HSD 2021-04-27 07613327354362 REUNION Stryker GmbH PHX 2021-04-27