Geistlich Derma-Gide™

GUDID 07610221013203

Geistlich Pharma AG

Collagen wound matrix dressing

• Primary Device ID: 07610221013203
• NIH Device Record Key: 0be327fd-60c3-4d9d-b687-a6040b8fc6dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geistlich Derma-Gide™
• Version Model Number: 500478
• Company DUNS: 480781728
• Company Name: Geistlich Pharma AG
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Outer Diameter: 14 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221013203 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182838

FDA Product Code

• KGN: Dressing, Wound, Collagen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-05-06
• Device Publish Date: 2019-01-31

On-Brand Devices [Geistlich Derma-Gide™]

• 07610221013227: 500480
• 07610221013210: 500479
• 07610221013203: 500478
• 07610221013197: 500477
• 07610221013180: 500476
• 07610221013173: 500475
• 07610221013166: 500474
• 07610221012626: 500427
• 07610221012619: 500426
• 07610221012602: 500425