Variobase C 062.4981

GUDID 07630031747044

Implantborne Elements

Institut Straumann AG

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07630031747044
• NIH Device Record Key: d465835b-7fe3-4ec6-8595-32a1170a4fec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Variobase C
• Version Model Number: RB/WB Variobase C, Ø3.8, GH 1.5, TAN
• Catalog Number: 062.4981
• Company DUNS: 483599259
• Company Name: Institut Straumann AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com
• Phone: +1(801)448-8168
• Email: info.usa@straumann.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07630031747044 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192742

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

[07630031747044]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-06
• Device Publish Date: 2021-03-29

On-Brand Devices [Variobase C]

• 07630031749024: Planning & Design Tools
• 07630031747068: Implantborne Elements
• 07630031747051: Implantborne Elements
• 07630031747044: Implantborne Elements
• 07630031707826: Implantborne Elements
• 07630031707819: Implantborne Elements
• 07630031707710: Implantborne Elements
• 07630031755230: Implantborne Elements
• 07630031755223: Implantborne Elements
• 07630031755216: Implantborne Elements
• 07630031771445: Implantborne Elements
• 07630031771438: Implantborne Elements