Geistlich Nexo-Gide®

GUDID 07610221014217

Geistlich Pharma AG

Tendon spacer

• Primary Device ID: 07610221014217
• NIH Device Record Key: 9e4941db-4586-4035-8ab2-cc73a58138a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geistlich Nexo-Gide®
• Version Model Number: 500663
• 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: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter
• Width: 30 Millimeter
• Height: 40 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221014217 [Primary]

FDA Product Code

• FTM: Mesh, Surgical

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: 2021-09-09
• Device Publish Date: 2021-09-01

On-Brand Devices [Geistlich Nexo-Gide®]

• 07610221014224: 500664
• 07610221014217: 500663
• 07610221014200: 500662