FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867395091 · Model: ABS-4403 · ARTHREX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Arthrex®
Primary DI
00888867395091
Version / Model
ABS-4403
Catalog Number
ABS-4403
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-01
Public Version
2
Public Version Date
2026-02-02
Public Version Status
Update
Public Device Record Key
7c19f70a-5ed2-482f-831e-ac7f61fbbb37

Device Description

SPEEDFLEX 25 x 30 x 1mm Presutured Graft

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
GAT Suture, nonabsorbable, synthetic, polyethylene
OWY Mesh, surgical, collagen, orthopaedics, reinforcement of tendon

GMDN Terms

Code Name
60907 Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial

Identifiers

Type ID
Primary 00888867395091

Customer Contacts