Implant Analog

GUDID 08809476188234

EBI Inc.

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08809476188234
• NIH Device Record Key: 5f825189-c86d-4887-98a9-6b0af5b8e1b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Implant Analog
• Version Model Number: OSR
• Company DUNS: 689515003
• Company Name: EBI Inc.
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809476188234 [Primary]

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-08
• Device Publish Date: 2017-11-22

On-Brand Devices [Implant Analog]

• 08809476188234: OSR
• 08809476186353: SLAS