Atlantis®

GUDID 07392532198830

Atlantis Conus Base Ti

DENTSPLY IH, INC.

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07392532198830
• NIH Device Record Key: 0073e09a-94ca-4aec-a0b3-d3f016a5735d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Atlantis®
• Version Model Number: 36331
• Company DUNS: 847337201
• Company Name: DENTSPLY IH, 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: false
• 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: +1(800)531-3481
• Email: implants-na-cs@dentsplysirona.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07392532198830 [Primary]

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[07392532198830]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2018-08-06

On-Brand Devices [Atlantis®]

• 07392532198854: Atlantis Conus Bridge Ti
• 07392532198847: Atlantis Conus Hybrid Ti
• 07392532198830: Atlantis Conus Base Ti
• 07392532198564: Atlantis Temp Crown
• 07392532177095: Atlantis® Insertion Guide