Arthrex®

FDA UDI

Class II (US FDA UDI)

by Arthrex, Inc.

Identity

Trade Name: Arthrex® FDA UDI
Generic Name: Total reverse shoulder prosthesis FDA UDI
Device Name: HUM INSERT L/42+3 TO FIT IN 42 CUP CONST FDA UDI
Model / Reference: AR-9503L-03C FDA UDI
Description: HUM INSERT L/42+3 TO FIT IN 42 CUP CONST FDA UDI

Identifiers

Catalog Number: AR-9503L-03C FDA UDI
Primary DI / UDI-DI: 00888867061224 FDA UDI
FDA Product Code: HRS FDA UDI
HWC FDA UDI
PHX FDA UDI
GMDN Term: Total reverse shoulder prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 FDA UDI
888.3660 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Total reverse shoulder prosthesis

Arthrex® by Arthrex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total reverse shoulder prosthesis.

Anatomical Shoulder# — Zimmer, Inc. · Class II
Shoulder Innovations Inset Reverse Total Shoulder — SHOULDER INNOVATIONS, Inc · Class II
R1 Reverse Shoulder System — CATALYST ORTHOSCIENCE Inc · Class II
DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
DELTA XTEND — DEPUY (IRELAND) · Class II
Tornier Flex Shoulder System — TORNIER, INC. · Class II
DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
AEQUALIS REVERSED FRACTURE — TORNIER, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Arthrex, Inc.

Sources (1)

FDA UDI 49f0a8ff-dd7c-45c8-ae30-941901f1d3b8 35 fields · synced May 30, 2026