FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867026766 · Model: AR-2323BSLM · ARTHREX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867026766
Version / Model
AR-2323BSLM
Catalog Number
AR-2323BSLM
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
22
Public Version Date
2024-02-01
Public Version Status
Update
Public Device Record Key
33a48b11-c985-4116-b472-be1ae0da6b6d

Device Description

BIO SWIVELOCK SP, 5.5x24.5MM

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

GMDN Terms

Code Name
45061 Tendon/ligament bone anchor, bioabsorbable

Identifiers

Type ID
Primary 00888867026766
Secondary M150AR2323BSLM1
Package 10888867026763

Customer Contacts