FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867498976 · Model: AR-5410T-AMGS-S · ARTHREX, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867498976
Version / Model
AR-5410T-AMGS-S
Catalog Number
AR-5410T-AMGS-S
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-01
Public Version
2
Public Version Date
2025-08-25
Public Version Status
Update
Public Device Record Key
f68ede00-534c-4430-8904-6eacb05c69fb

Device Description

VIP™ Augmented MGS Reamer, Locking, S

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
No
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
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
QHE Shoulder arthroplasty implantation system
PHX shoulder prosthesis, reverse configuration
LLZ System, image processing, radiological

GMDN Terms

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

Identifiers

Type ID
Primary 00888867498976

Customer Contacts