FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867301962 · Model: AR-7292 · ARTHREX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Arthrex®
Primary DI
00888867301962
Version / Model
AR-7292
Catalog Number
AR-7292
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-13
Public Version
2
Public Version Date
2025-11-11
Public Version Status
Update
Public Device Record Key
d4f30bdd-82c1-49ba-a671-c69f594a9d1b

Device Description

SuturePatch Trapezoid, 45 x 35mm

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
OWX Mesh, surgical, non-absorbable, orthopaedics, reinforcement of tendon
FTL Mesh, surgical, polymeric

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Package 10888867301969
Primary 00888867301962

Customer Contacts