Home GUDID 00887868459931
Comprehensive® Reverse Shoulder
Primary DI 00887868459931
Brand Comprehensive® Reverse Shoulder
Company Biomet Orthopedics, LLC
Model 010001827
Catalog number 010001827
Published 2021-09-26
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 KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED PAO prosthesis, shoulder, semi-constrained, metal/polymer + additive, cemented PHX shoulder prosthesis, reverse configuration
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented Orthopedic 2 PAO Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented Orthopedic 2 PHX Shoulder Prosthesis, Reverse Configuration Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00887868459931 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 00887868459931 00887868459931 887868459931 0887868459931
GMDN Terms# Term, Definition table Term Definition Hand-held surgical retractor, reusable A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not dedicated to ophthalmic surgery or small nerve/vessel retraction, but may otherwise be clinically dedicated. It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 129278169 Device count 1 Lot or batch true 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 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 07613327354331 REUNION Stryker GmbH KWS 2022-11-15 07613327354355 REUNION Stryker GmbH KWS 2022-11-15 07613327354805 REUNION Stryker GmbH KWS 2022-11-15 07613327354904 REUNION Stryker GmbH KWS 2022-11-15 07613327354935 REUNION Stryker GmbH KWS 2022-11-15 07613327354942 REUNION Stryker GmbH KWS 2022-11-15 07613327355024 REUNION Stryker GmbH KWS 2022-11-15 07613327355093 REUNION Stryker GmbH KWS 2022-11-15 07613327355109 REUNION Stryker GmbH KWS 2022-11-15 07613327355222 REUNION Stryker GmbH KWS 2022-11-15 07613327355246 REUNION Stryker GmbH KWS 2022-11-15 07613327355260 REUNION Stryker GmbH KWS 2022-11-15 07613327355291 REUNION Stryker GmbH KWS 2022-11-15 07613327355345 REUNION Stryker GmbH KWS 2022-11-15 07613327355369 REUNION Stryker GmbH KWS 2022-11-15