OsseoGuard Flex

GUDID 00813954020365

Resorbable Collagen Membrane for Dental Surgery 20mm x 30mm

COLLAGEN MATRIX, INC.

Collagen dental regeneration membrane

• Primary Device ID: 00813954020365
• NIH Device Record Key: a61cb383-e7de-4f91-b058-790b70a85608
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OsseoGuard Flex
• Version Model Number: OGF2030
• Company DUNS: 176262442
• Company Name: COLLAGEN MATRIX, 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Width: 20 Millimeter
• Width: 20 Millimeter
• Width: 20 Millimeter
• Width: 20 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813954020365 [Primary]

FDA Product Code

• NPL: Barrier, Animal Source, Intraoral

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: 2018-03-29
• Device Publish Date: 2015-10-22

On-Brand Devices [OsseoGuard Flex]

• 00813954020372: Resorbable Collagen Membrane for Dental Surgery 30mm x 40mm
• 00813954020365: Resorbable Collagen Membrane for Dental Surgery 20mm x 30mm
• 00813954020358: Resorbable Collagen Membrane for Dental Surgery 15mm x 20mm
• 00813954027418: Resorbable Collagen Membrane
• 00813954027401: Resorbable Collagen Membrane
• 00813954027395: Resorbable Collagen Membrane