Morpheus 012-MOR

GUDID 00812593020651

12cc Morpheus

BIOGENNIX LLC

Synthetic bone graft

• Primary Device ID: 00812593020651
• NIH Device Record Key: 98f3b0e2-8780-413f-9578-54664453aa48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Morpheus
• Version Model Number: 012-MOR
• Catalog Number: 012-MOR
• Company DUNS: 021486533
• Company Name: BIOGENNIX LLC
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00812593020651 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142828

FDA Product Code

• MQV: Filler, Bone Void, Calcium Compound

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-19

On-Brand Devices [Morpheus]

• 00812593020668: 9cc Morpheus
• 00812593020651: 12cc Morpheus
• 00812593020644: 6cc Morpheus
• 00812593020637: 3cc Morpheus