Atlas Implant System

GUDID 07350081495008

Dentatus Atlas Implant, blister pack including 1 pc

Dentatus AB

Transgingival implant

• Primary Device ID: 07350081495008
• NIH Device Record Key: 06eaeefe-892b-4866-a16b-b500fc7f6c75
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Atlas Implant System
• Version Model Number: AT-24L
• Company DUNS: 355803412
• Company Name: Dentatus AB
• 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

Customer Support Contacts

• Phone: +46854650900
• Email: info@dentatus.se

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350081494568 [Package]; Package: Implant pack [2 Units]; In Commercial Distribution
GS1	07350081495008 [Primary]

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

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: 2015-08-07

On-Brand Devices [Atlas Implant System ]

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• 07350081495008: Dentatus Atlas Implant, blister pack including 1 pc
• 07350081494995: Dentatus Atlas Implant, blister pack including 1 pc
• 07350081494988: Dentatus Atlas Implant, blister pack including 1 pc
• 07350081494971: Dentatus Atlas Implant, blister pack including 1 pc
• 07350081494964: Dentatus Atlas Implant System, blister pack including 1 pc
• 07350081494957: Dentatus Atlas Implant, blister pack including 1 pc
• 07350081494940: Dentatus Atlas Implant, blister pack including 1pc