FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867521780 · Model: 8039-000 · 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
00888867521780
Version / Model
8039-000
Catalog Number
8039-000
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-25
Public Version
1
Public Version Date
2025-10-03
Public Version Status
New
Public Device Record Key
a4e7b9d4-574d-49d1-8502-c071afa6b3a6

Device Description

7.0mm Flat Washer

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HTN WASHER, BOLT NUT
HWC Screw, fixation, bone

GMDN Terms

Code Name
61670 Implantable bone washer

Identifiers

Type ID
Primary 00888867521780

Customer Contacts