FDA UDI In Commercial Distribution 🇺🇸 United States

Glenoid IRI Leg (23mm)

DI: 00811813020174 · Model: L · CUSTOM ORTHOPAEDIC SOLUTIONS, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Glenoid IRI Leg (23mm)
Primary DI
00811813020174
Version / Model
L
Catalog Number
0006-0005-23
Company Name
CUSTOM ORTHOPAEDIC SOLUTIONS, INC.
Labeler DUNS
078667390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-02
Public Version
6
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
9978ab7c-c097-49f4-a0c7-4a9d518606fd

Device Description

The Glenoid IRI Leg (23mm) is a component of the Glenoid Intelligent Reusable Instrument (IRI). The Glenoid IRI Leg (23mm) is indicated for use as part of the Arthrex Glenoid Intelligent Reusable Instrument System (IRIS) for Total Shoulder Arthroplasty (TSA).

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
PHX Shoulder Prosthesis, Reverse Configuration

GMDN Terms

Code Name
59009 Orthopaedic implant/instrument assembling device
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00811813020174

Customer Contacts

Phone
2168005905

Device Sizes

Type Value Unit Text
Length 23 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry, dark, cool place