FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867242081 · Model: AR-1530P-CP · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867242081
Version / Model
AR-1530P-CP
Catalog Number
AR-1530P-CP
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-06
Public Version
7
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
82b9cce5-40c0-492a-9bd9-9eb650595d04

Device Description

Forefoot IB Implant Sys, PEEK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Secondary AR1530PCP1
Primary 00888867242081

Customer Contacts