FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867409750 · Model: AR-5410-AMGS-M · ARTHREX, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867409750
Version / Model
AR-5410-AMGS-M
Catalog Number
AR-5410-AMGS-M
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-24
Public Version
3
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
b218958e-fedc-421a-9074-d100cf3a299b

Device Description

VIP™ Glenoid Reamer, Augmented MGS Med.

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LLZ System, image processing, radiological
PHX shoulder prosthesis, reverse configuration
QHE Shoulder arthroplasty implantation system
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
61807 Bone-resection orthopaedic reamer, single-use

Identifiers

Type ID
Primary 00888867409750

Customer Contacts