FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867062276 · Model: AR-9540SM-INF · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867062276
Version / Model
AR-9540SM-INF
Catalog Number
AR-9540SM-INF
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-02
Public Version
5
Public Version Date
2024-02-29
Public Version Status
Update
Public Device Record Key
b040ec2f-cb1f-4f38-bec1-b7eed566259a

Device Description

UNIVERS REVS TRL GLENOSPHERE 36+2.5 INF

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
60931 Reverse shoulder head prosthesis trial

Identifiers

Type ID
Primary 00888867062276

Customer Contacts