naturesQue MaxOss P

GUDID 00813954023472

Anorganic Bone Mineral

COLLAGEN MATRIX, INC.

Dental bone matrix implant, animal-derived

• Primary Device ID: 00813954023472
• NIH Device Record Key: 444b086e-ef0a-4486-90e6-cf3e685c26e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: naturesQue MaxOss P
• Version Model Number: 58493
• 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

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813954023472 [Primary]

FDA Product Code

• NPM: Bone Grafting Material, Animal Source

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-04
• Device Publish Date: 2020-02-25

On-Brand Devices [naturesQue MaxOss P]

• 00813954023496: Anorganic Bone Mineral in Syringe
• 00813954023489: Anorganic Bone Mineral in Syringe
• 00813954023472: Anorganic Bone Mineral
• 00813954023465: Anorganic Bone Mineral
• 00813954023458: Anorganic Bone Mineral
• 00813954023441: Anorganic Bone Mineral
• 00813954023434: Anorganic Bone Mineral
• 00813954023427: Anorganic Bone Mineral