EzDebride

GUDID 10860010005917

This DI information is for the EzDebride Shipper containing 80 devices

Mdm Wound Ventures Inc.

Wound debridement pad

• Primary Device ID: 10860010005917
• NIH Device Record Key: dc9bfded-a622-432f-8de2-41230869d37e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EzDebride
• Version Model Number: EZ-001
• Company DUNS: 080191736
• Company Name: Mdm Wound Ventures Inc.
• Device Count: 80
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860010005903 [Unit of Use]
GS1	10860010005917 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-08
• Device Publish Date: 2023-05-31

On-Brand Devices [EzDebride]

• 10860010005917: This DI information is for the EzDebride Shipper containing 80 devices
• 00860010005903: EzDebride Carton containing 8 EzDebride devices, unit of use.