FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867261648 · Model: AR-3200-1049 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867261648
Version / Model
AR-3200-1049
Catalog Number
AR-3200-1049
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-16
Public Version
1
Public Version Date
2022-08-24
Public Version Status
New
Public Device Record Key
7425f190-7805-49e1-918a-e9c4f9f8f638

Device Description

Synergy Matrix Management SW Addtnl Lic

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OUG Medical device data system

GMDN Terms

Code Name
60723 Medical image management system

Identifiers

Type ID
Primary 00888867261648

Customer Contacts