EzDebride

Basic Information

• Brand Name: EzDebride
• Primary DI: 10860010005917
• Version / Model: EZ-001
• Company Name: Mdm Wound Ventures Inc.
• Labeler DUNS: 080191736
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 80
• Record Status: Published
• Publish Date: 2023-05-31
• Public Version: 1
• Public Version Date: 2023-06-08
• Public Version Status: New
• Public Device Record Key: dc9bfded-a622-432f-8de2-41230869d37e

Device Description

This DI information is for the EzDebride Shipper containing 80 devices

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: Yes
• 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
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	878.4800	1

GMDN Terms

Code	Name	Definition	Implantable	Status
58294	Wound debridement pad	A sterile device intended to be used for the manual debridement of wounds (e.g., diabetic foot ulcers, venous ulcers, arterial ulcers, pressure ulcers, bedsores) by gentle wiping of the wound surface to remove unhealthy tissue (e.g., exudate, slough, cellular debris) to promote healing. It typically consists of a swab-like pad with the side to be used for debridement made of synthetic polymer (e.g., monofilament polyester) fibres. It may be soaked in water/saline before use. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	10860010005917	GS1
Unit of Use	00860010005903	GS1