FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867424050 · Model: AR-10920F · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Arthrex®
Primary DI
00888867424050
Version / Model
AR-10920F
Catalog Number
AR-10920F
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-06
Public Version
3
Public Version Date
2026-02-09
Public Version Status
Update
Public Device Record Key
8d1866c4-2030-4ad7-9f49-443ac8eab1b1

Device Description

Nano Suction Biter 70mm Flat Tip 5 PK

Device Characteristics

Single Use
No
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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Package 10888867424057
Primary 00888867424050

Customer Contacts