FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867014695 · Model: AR-1370P · ARTHREX, INC.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867014695
Version / Model
AR-1370P
Catalog Number
AR-1370P
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
24
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
d1cb2328-8798-4ae4-bad2-7a518cfce51f

Device Description

PEEK INTERF SCRW W/DISP SHTH 7X 23MM

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 Safe
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
MBI Fastener, fixation, nondegradable, soft tissue

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 00888867014695
Secondary M150AR1370P1

Customer Contacts