KMEDIC

Basic Information

• Brand Name: KMEDIC
• Primary DI: 24026704281040
• Version / Model: IPN014727
• Catalog Number: KM49090
• Company Name: TELEFLEX INCORPORATED
• Labeler DUNS: 002348191
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2018-09-15
• Public Version: 2
• Public Version Date: 2021-11-16
• Public Version Status: Update
• Public Device Record Key: 2a3c0a9c-45f8-45b5-8916-2d7d9ac17645

Device Description

LEAD HAND ADULT 14"

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: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: Yes
• Sterilization Methods: Moist Heat or Steam Sterilization

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
GAD	RETRACTOR	General, Plastic Surgery	878.4800	1

GMDN Terms

Code	Name	Definition	Implantable	Status
44214	Orthosis suspension unit	A component of an orthosis that holds the orthosis to the body at various anatomical sites, e.g., the pelvis or malleolus. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	24026704281040	GS1
Direct Marking	04026704281046	GS1

Customer Contacts

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