FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867062580 · Model: AR-9610 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867062580
Version / Model
AR-9610
Catalog Number
AR-9610
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
23
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
a8d5cb09-6e04-46fc-9a7c-329acd7e8ee6

Device Description

DISPOSABLE PENCIL KIT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 00888867062580
Secondary M150AR96101
Package 10888867062587

Customer Contacts