FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 10888867241401 · Model: AR-8964-22 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Arthrex®
Primary DI
10888867241401
Version / Model
AR-8964-22
Catalog Number
AR-8964-22
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-12-03
Public Version
1
Public Version Date
2021-12-13
Public Version Status
New
Public Device Record Key
63241853-f40d-4a11-8d5f-063c6f3a715c

Device Description

End Cap, Screws

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
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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
48011 External orthopaedic fixation system, single-use

Identifiers

Type ID
Unit of Use 00888867241404
Secondary M150AR8964220
Primary 10888867241401

Customer Contacts