ELLIPTIC MATRIX 048.456

GUDID 07630031724694

Elliptical matrix, D 3.6mm, H 3.2mm, Elitor®/Ti

Institut Straumann AG

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07630031724694
• NIH Device Record Key: 67fce8b5-2504-4682-9245-47bd1705d6bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ELLIPTIC MATRIX
• Version Model Number: Edentulous Abutments
• Catalog Number: 048.456
• Company DUNS: 483599259
• Company Name: Institut Straumann 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: 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)448-8168
• Email: info.usa@straumann.com

Device Dimensions

• Outer Diameter: 3.6 Millimeter
• Outer Diameter: 3.6 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07630031724694 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040539

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[07630031724694]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-09-24

On-Brand Devices [ELLIPTIC MATRIX]

• 07630031724700: Spare lamella retention insert, H 2.6mm, Elitor®
• 07630031724694: Elliptical matrix, D 3.6mm, H 3.2mm, Elitor®/Ti