FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867028036 · Model: AR-2923PS · ARTHREX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867028036
Version / Model
AR-2923PS
Catalog Number
AR-2923PS
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-15
Public Version
27
Public Version Date
2024-02-01
Public Version Status
Update
Public Device Record Key
1184c4f8-6bbf-4e38-b0f9-7b8848356f11

Device Description

SUTR ANCH,PEEK P-LCK,2.9X 12.5MM

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
MR Safe
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
MAI FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
HWC Screw, fixation, bone

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 00888867028036
Secondary M150AR2923PS1
Package 10888867028033

Customer Contacts