infinity OCTAGON BL RC Healing abutment, conical Ø 6.5 mm GH 2.0 mm 5022093

GUDID E0HM50220931

BL RC Healing abutment, conical Ø 6.5 mm GH 2.0 mm for infinity OCTAGON Dental Implant BL RC

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Screw endosteal dental implant, two-piece

• Primary Device ID: E0HM50220931
• NIH Device Record Key: f122caf5-25e3-48d2-9211-641ce526beb2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: infinity OCTAGON BL RC Healing abutment, conical Ø 6.5 mm GH 2.0 mm
• Version Model Number: 5022093
• Catalog Number: 5022093
• Company DUNS: 318034329
• Company Name: Hager & Meisinger Gesellschaft mit beschränkter Haftung
• 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(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com
• Phone: +1(508)588-3100
• Email: kathystrange@acesurgical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E0HM50220931 [Primary]
HIBCC	E0HM50220939 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143539

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

[E0HM50220931]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-02-15
• Device Publish Date: 2017-02-13

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