FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867543645 · Model: 76-20401 · ARTHREX, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Arthrex®
Primary DI
00888867543645
Version / Model
76-20401
Catalog Number
76-20401
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-13
Public Version
1
Public Version Date
2026-03-23
Public Version Status
New
Public Device Record Key
4a68596b-257e-43e5-b4c3-0142d945aae8

Device Description

Smooth Wire 2.0x400mm, Bayonet Tip

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
HTY PIN, FIXATION, SMOOTH
OSN Software for diagnosis/treatment

GMDN Terms

Code Name
67571 External orthopaedic fixation system noninvasive component, single-use

Identifiers

Type ID
Primary 00888867543645

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190069 000