creos™ xenoprotect

GUDID 04250830900070

collagen membrane

Matricel GmbH

Collagen dental regeneration membrane

• Primary Device ID: 04250830900070
• NIH Device Record Key: 37a0ca10-65d1-4d83-b286-36c0f503d25b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: creos™ xenoprotect
• Version Model Number: N3040
• Company DUNS: 344166512
• Company Name: Matricel GmbH
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49240756440
• Email: info@matricel.de

Device Dimensions

• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250830900070 [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: 2015-08-31

On-Brand Devices [creos™ xenoprotect]

• 04250830900070: collagen membrane
• 04250830900063: collagen membrane
• 04250830900056: collagen membrane