Geistlich Bio-Oss Pen®

GUDID 07610221010523

Geistlich Pharma AG

Dental bone matrix implant, animal-derived

• Primary Device ID: 07610221010523
• NIH Device Record Key: 4fc07cab-574d-4c7d-9872-21362f4a483a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geistlich Bio-Oss Pen®
• Version Model Number: 20126
• Company DUNS: 480781728
• Company Name: Geistlich Pharma AG
• 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

• Weight: 0.5 Gram
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221010523 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-09
• Device Publish Date: 2015-09-01

On-Brand Devices [Geistlich Bio-Oss Pen®]

• 07610221010523: 20126
• 07610221010509: 20116
• 07610221010493: 20115