FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867247116 · Model: AR-8967KS · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867247116
Version / Model
AR-8967KS
Catalog Number
AR-8967KS
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-28
Public Version
4
Public Version Date
2021-04-20
Public Version Status
Update
Public Device Record Key
cef53226-84e2-4f05-b763-d381aca7e4cc

Device Description

GUIDE WIRE, 2.4 MM X 203 MM, STRL

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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
57874 Suturing unit, single-use

Identifiers

Type ID
Primary 00888867247116

Customer Contacts