Geistlich Bio-Oss® Block

GUDID 07610221010363

Geistlich Pharma AG

Dental bone matrix implant, animal-derived

• Primary Device ID: 07610221010363
• NIH Device Record Key: 4ec2eb54-3b8d-4e23-9aa5-ed09dfc6e7c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geistlich Bio-Oss® Block
• Version Model Number: 20131
• 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

• Depth: 1 Centimeter
• Width: 1 Centimeter
• Height: 2 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221010363 [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: 2018-08-08
• Device Publish Date: 2015-09-01

Devices Manufactured by Geistlich Pharma AG

• 07610221015481 - Geistlich Fibro-Gide®: 2022-09-19
• 07610221015498 - Geistlich Fibro-Gide®: 2022-09-19
• 07610221071906 - Wound Matrix PLUS: 2022-09-19
• 07610221071913 - Wound Matrix PLUS: 2022-09-19
• 07610221014200 - Geistlich Nexo-Gide®: 2021-09-09
• 07610221014217 - Geistlich Nexo-Gide®: 2021-09-09
• 07610221014224 - Geistlich Nexo-Gide®: 2021-09-09
• 07610221015320 - Geistlich Bio-Oss®: 2021-06-23