Arthrex®

Basic Information

• Brand Name: Arthrex®
• Primary DI: 00888867021518
• Version / Model: AR-1812
• Catalog Number: AR-1812
• Company Name: ARTHREX, INC.
• Labeler DUNS: 131747628
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2018-07-26
• Public Version: 5
• Public Version Date: 2024-02-28
• Public Version Status: Update
• Public Device Record Key: e2b5fd9d-e1fc-4812-9271-c6b5227968e8

Device Description

BACKFLOW CAP

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	Medical Specialty	Regulation #	Device Class
LXH	ORTHOPEDIC MANUAL SURGICAL INSTRUMENT	Orthopedic	888.4540	1

GMDN Terms

Code	Name	Definition	Implantable	Status
45190	Bone tunnel plug, non-cannulated	A device typically intended to prevent irrigation fluid from exiting the knee joint via the tibial tunnel [a channel drilled through the knee joint during anterior cruciate ligament (ACL) repair] to maintain visualization of the joint during arthroscopy. The device typically has a rounded cap at the proximal end and tapers distally; it is not cannulated. It is inserted manually into the tunnel, is available in a variety of diameters, and is made of hard plastic. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00888867021518	GS1
Package	10888867021515	GS1	Box	10	In Commercial Distribution

Customer Contacts

• Phone: [phone]
• Email: [email protected]