Geistlich Bio-Gide®

GUDID 07610221010417

Geistlich Pharma AG

Collagen dental regeneration membrane

• Primary Device ID: 07610221010417
• NIH Device Record Key: ed891fe5-a4a6-40f4-9a15-ded2d2959815
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geistlich Bio-Gide®
• Version Model Number: 20152
• 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

• Width: 25 Millimeter
• Height: 25 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221010417 [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: 2015-09-01

On-Brand Devices [Geistlich Bio-Gide®]

• 07610221010424: 20153
• 07610221010417: 20152
• 07610221010400: 20151
• 07610221014309: 500710