Geistlich Combi-Kit Collagen

GUDID 07610221010370

Geistlich Pharma AG

Collagen dental regeneration membrane

• Primary Device ID: 07610221010370
• NIH Device Record Key: 2ef4a524-1d3f-47b0-afce-c83d58fbcfde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geistlich Combi-Kit Collagen
• Version Model Number: 20146
• 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: true
• 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	07610221010370 [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: 3
• Public Version Date: 2018-08-09
• 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