FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867215672 · Model: AR-9300OBT · ARTHREX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867215672
Version / Model
AR-9300OBT
Catalog Number
AR-9300OBT
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-15
Public Version
8
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
4b91b676-86da-4769-920a-1a1bf63fefe1

Device Description

BURR, OVAL, 10 FLUTE, 3.0MM

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
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
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
36249 Orthopaedic bur, reusable

Identifiers

Type ID
Primary 00888867215672
Secondary M150AR9300OBT1
Package 10888867215679

Customer Contacts