FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867138360 · Model: AR-9260-32 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867138360
Version / Model
AR-9260-32
Catalog Number
AR-9260-32
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-10
Public Version
6
Public Version Date
2021-12-07
Public Version Status
Update
Public Device Record Key
5e94b022-95c4-41cf-934c-227fcc5569a2

Device Description

FUKUDA RETRTR,7 1/2"X38MMX 81MMT-HNDL

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
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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00888867138360

Customer Contacts