Unite Medical®

Basic Information

• Brand Name: Unite Medical®
• Primary DI: 00850012035640
• Version / Model: Heel Stabilizer (XLarge)
• Catalog Number: HS3170-XL
• Company Name: Unite Medical, LLC
• Labeler DUNS: 117553945
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-12-28
• Public Version: 1
• Public Version Date: 2024-01-05
• Public Version Status: New
• Public Device Record Key: edd22ede-8609-4d45-8dc7-febbfe41a6c2

Device Description

The Unite Medical® heel stabilizer is designed with medical grade silicone combined with a soft gel center providing pain relief to the heel region. The heel stabilizer helps to reduce pain associated with Achilles tendinitis, plantar fasciitis, heel and calcaneal spurs as well as providing additional load & vibration relief for arthritis in the knee and leg joints.

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• 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: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
ITW	Joint, Ankle, External Brace	Physical Medicine	890.3475	1

GMDN Terms

Code	Name	Definition	Implantable	Status
35547	Heel stirrup cushion/pad	A pad designed to be placed between a patient's foot and a table heel stirrup, cushioning the patient's heel and lower leg to provide greater comfort and to reduce the risk of sores during long procedures. The device is typically made of soft material (e.g., foam) with an appropriate shape and size to fit the heel stirrup; it is usually supplied in pairs. The device is used mainly for patients in lithotomic position for obstetrical, urological, colonic, or rectal procedures. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00850012035640	GS1

Customer Contacts

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