FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867133808 · Model: AR-8970-09T · ARTHREX, INC.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867133808
Version / Model
AR-8970-09T
Catalog Number
AR-8970-09T
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
26
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
559025b6-5239-4408-b8a5-bff7bf37b6f1

Device Description

LARGE BB-TAK, THREADED

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
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
HRS PLATE, FIXATION, BONE
HTN WASHER, BOLT NUT
HWC Screw, fixation, bone

GMDN Terms

Code Name
32854 Orthopaedic bone pin, non-bioabsorbable

Identifiers

Type ID
Primary 00888867133808
Secondary M150AR897009T0

Customer Contacts