DuraMatrix-Onlay Conform DMOC22

GUDID 00813954026091

Collagen Dural Regeneration Matrix

COLLAGEN MATRIX, INC.

Dura mater graft, bovine

• Primary Device ID: 00813954026091
• NIH Device Record Key: e98da2ca-aed5-466f-a4af-a6b9f30f568d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DuraMatrix-Onlay Conform
• Version Model Number: DMOC22
• Catalog Number: DMOC22
• 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

Customer Support Contacts

• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com
• Phone: (800) 962 6558
• Email: cmf-custserv@stryker.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813954026091 [Primary]

FDA Product Code

• GXQ: Dura Substitute

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: 2024-10-28
• Device Publish Date: 2024-02-22

On-Brand Devices [DuraMatrix-Onlay Conform]

• 00813954026114: Collagen Dural Regeneration Matrix
• 00813954026107: Collagen Dural Regeneration Matrix
• 00813954026091: Collagen Dural Regeneration Matrix
• 00813954026084: Collagen Dural Regeneration Matrix
• 00813954026077: DMOC11