FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867039001 · Model: AR-6200 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Arthrex®
Primary DI
00888867039001
Version / Model
AR-6200
Catalog Number
AR-6200
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-04
Public Version
1
Public Version Date
2024-11-12
Public Version Status
New
Public Device Record Key
58b199c7-1e68-4341-ac77-f5c24a54553b

Device Description

Y-INFLOW TUBING, 7.0MM

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
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
HRX Arthroscope

GMDN Terms

Code Name
44772 Cardiac ablation system irrigation tubing set

Identifiers

Type ID
Package 10888867039008
Primary 00888867039001

Customer Contacts