Procellera Composite VHR-0506

GUDID 00894318002470

Procellera Composite Rx; 5"x6"

Vomaris Wound Care, Inc.

Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing Bioelectric wound dressing

• Primary Device ID: 00894318002470
• NIH Device Record Key: 39387b8f-786c-49a4-8296-b6ae7bc993fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procellera Composite
• Version Model Number: 5"x6"
• Catalog Number: VHR-0506
• Company DUNS: 080126901
• Company Name: Vomaris Wound Care, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com
• Phone: (480) 921-4948
• Email: customerservice@vomaris.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00894318002470 [Primary]
GS1	10894318002477 [Package]; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180533

FDA Product Code

• FRO: Dressing, Wound, Drug

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: 2022-11-28
• Device Publish Date: 2022-11-18

On-Brand Devices [Procellera Composite]

• 00894318002517: Procellera Composite Rx; 2.5" diameter
• 00894318002494: Procellera Composite Rx; 4' diameter
• 00894318002487: Procellera Composite Rx; 4"x4"
• 00894318002470: Procellera Composite Rx; 5"x6"
• 00894318002463: Procellera Composite Rx; 4.5"x10"
• 00894318002456: Procellera Composite Rx; 6"x11.5"
• 00810198030419: Procellera Composite OTC; 4' diameter
• 00810198030402: Procellera Composite OTC; 4"x4"
• 00810198030198: Procellera Composite Rx; 4.2"x7.5"
• 00810198030181: Procellera Composite Rx; 4.4"x9.6"