Home GUDID 00811596031916 Reverse Shoulder System
Primary DI 00811596031916
Brand Reverse Shoulder System
Company CATALYST ORTHOSCIENCE INC.
Model 1230-7524-002
Catalog number 1230-7524-002
Device description Catalyst Humeral Stem – Long 41mm
Published 2026-07-17
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented 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 PHX Shoulder Prosthesis, Reverse Configuration Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00811596031916 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 00811596031916 00811596031916 811596031916 0811596031916
GMDN Terms# Term, Definition table Term Definition Total reverse shoulder prosthesis A sterile implantable artificial substitute for a shoulder joint designed to replace both articulating surfaces of the joint particularly in patients with chronic, longstanding rotator cuff muscle tears, arthritis, and/or humeral fractures unsuccessfully treated by previous surgery. The device reverses normal anatomy so that the head portion of the joint is attached to the scapula and the socket portion is attached to the humerus. It typically includes a humeral stem and glenosphere (head) with body and cup components. The device may include screws for implantation and may be implanted with or without bone cement.
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 false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 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 00811596031923 Reverse Shoulder System 1230-7513-003 1230-7513-003 2026-07-17 00811596031930 Reverse Shoulder System 1230-7514-003 1230-7514-003 2026-07-17 00811596031947 Reverse Shoulder System 1230-7525-001 1230-7525-001 2026-07-17 00811596031954 Reverse Shoulder System 1230-4313 1230-4313 2026-07-17 00811596031961 CSR Shoulder System 1226-5038-001 1226-5038-001 2026-07-17 00811596031978 CSR Shoulder System 1226-5038-002 1226-5038-002 2026-07-17 00811596031985 CSR Shoulder System 1226-5038-003 1226-5038-003 2026-07-17 00811596031992 EA Convertible System 1231-4605 1231-4605 2026-07-17 00811596032005 Reverse Shoulder System 1230-4224-003 1230-4224-003 2026-07-17 00811596032012 Reverse Shoulder System 1230-4225-003 1230-4225-003 2026-07-17 00811596031695 EA Convertible System 1231-4601-001 1231-4601-001 2026-07-14 00811596031701 EA Convertible System 1231-4601-002 1231-4601-002 2026-07-14 00811596031718 EA Convertible System 1231-4601-003 1231-4601-003 2026-07-14 00811596031725 EA Convertible System 1231-4601-004 1231-4601-004 2026-07-14 00811596031732 EA Convertible System 1231-4601-005 231-4601-005 2026-07-14 00811596031749 EA Convertible System 1231-4601-006 1231-4601-006 2026-07-14 00811596031657 EA Convertible System 1231-4603-001 1231-4603-001 2026-07-13
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