AccessGUDID - DEVICE: Arthrex® (00888867295872)

GUDID

Device Identifier (DI) Information

Brand Name: Arthrex®
Version or Model: AR-9564-T2436-LAT
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: AR-9564-T2436-LAT
Company Name: ARTHREX, INC.

Primary DI Number: 00888867295872
Issuing Agency: GS1
Commercial Distribution End Date: June 26, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 131747628 *Terms of Use

Device Description: 36 +4 LAT/24 Ti Glenosphere

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
48093	Reverse shoulder prosthesis head	A sterile component of a reverse shoulder prosthesis that consists of a hemisphere-shaped metal or combined metal/polyethylene piece (glenosphere) intended to be attached to the reverse shoulder base plate, or directly to the glenoid fossa of the scapula, to articulate with the reverse shoulder cup.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
PHX	shoulder prosthesis, reverse configuration

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 141d757b-b370-4130-8cd9-f4a334372eac
Public Version Date: November 24, 2021
Public Version Number: 4
DI Record Publish Date: August 20, 2018