FDA UDI Not in Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867266841 · Model: AR-8952DFM-S · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867266841
Version / Model
AR-8952DFM-S
Catalog Number
AR-8952DFM-S
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-01
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
4ca508d1-9e01-4ae9-9c79-3c3218b34ec5
Distribution End Date
2021-06-26

Device Description

Dorsal Midfoot Fusion Plate,3mm,Med,Ster

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
HWC Screw, fixation, bone

GMDN Terms

Code Name
61688 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Identifiers

Type ID
Secondary M150AR8952DFMS1
Primary 00888867266841

Customer Contacts