Home GUDID 00811596032036 Reverse Shoulder System
Primary DI 00811596032036
Brand Reverse Shoulder System
Company CATALYST ORTHOSCIENCE INC.
Model 1230-5216
Catalog number 1230-5216
Device description Flex Baseplate Inserter
Published 2026-08-18
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name PHX Shoulder Prosthesis, Reverse Configuration
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class PHX Shoulder Prosthesis, Reverse Configuration Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00811596032036 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 00811596032036 00811596032036 811596032036 0811596032036
GMDN Terms# Term, Definition table Term Definition Orthopaedic prosthesis implantation positioning instrument, reusable A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 079702565 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 true 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# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00811596032050 Reverse Shoulder System 1230-7506-002 1230-7506-002 2026-08-18 00811596032067 Reverse Shoulder System 1230-7507-002 1230-7507-002 2026-08-18 00811596032074 Reverse Shoulder System 1230-7525-002 1230-7525-002 2026-08-18 00811596032081 Reverse Shoulder System 1230-7526-001 1230-7526-001 2026-08-18 00811596032098 Reverse Shoulder System 1230-7526-002 1230-7526-002 2026-08-18 00811596032104 Reverse Shoulder System 1230-7527-001 1230-7527-001 2026-08-18 00811596032111 Reverse Shoulder System 1230-7527-002 1230-7527-002 2026-08-18 00811596032128 Reverse Shoulder System 1230-7528-001 1230-7528-001 2026-08-18 00811596032135 Reverse Shoulder System 1230-7528-002 1230-7528-002 2026-08-18 00811596032142 Reverse Shoulder System 1230-7529-001 1230-7529-001 2026-08-18 00811596032159 Reverse Shoulder System 1230-7529-002 1230-7529-002 2026-08-18 00811596032166 Reverse Shoulder System 1230-7530-001 1230-7530-001 2026-08-18 00811596032173 Reverse Shoulder System 1230-7530-002 1230-7530-002 2026-08-18 00811596032180 Reverse Shoulder System 1230-7531-001 1230-7531-001 2026-08-18 00811596032197 Reverse Shoulder System 1230-7531-002 1230-7531-002 2026-08-18 00811596031886 Reverse Shoulder System 1230-7523-001 1230-7523-001 2026-07-17 00811596031893 Reverse Shoulder System 1230-7523-002 1230-7523-002 2026-07-17 00811596031909 Reverse Shoulder System 1230-7524-001 1230-7524-001 2026-07-17 00811596031916 Reverse Shoulder System 1230-7524-002 1230-7524-002 2026-07-17 00811596031923 Reverse Shoulder System 1230-7513-003 1230-7513-003 2026-07-17
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