DermaView

GUDID 00714196392343

DERMARITE INDUSTRIES LLC

Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive

• Primary Device ID: 00714196392343
• NIH Device Record Key: c9c54cd7-1622-4337-a382-2d65154778e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaView
• Version Model Number: 00241E
• Company DUNS: 883925562
• Company Name: DERMARITE INDUSTRIES LLC
• Device Count: 1
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00714196392343 [Primary]

FDA Product Code

• KMK: Device, Intravascular Catheter Securement

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: 2021-09-17
• Device Publish Date: 2021-09-09

On-Brand Devices [DermaView]

• 00714196251459: 00251E
• 00714196241238: 00241E
• 00714196392381: 00251E
• 00714196392343: 00241E