OKTAGON BL RC Healing abutment Ø 7.0 mm GH 4.0 mm 22123

GUDID EDRS221231

BL RC Healing abutment Ø 7.0 mm GH 4.0 mm for OKTAGON Dental Implant BL RC

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Screw endosteal dental implant, two-piece

• Primary Device ID: EDRS221231
• NIH Device Record Key: 6d4344f7-df67-4842-82a2-3d91265b718a
• Commercial Distribution Discontinuation: 2018-09-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: OKTAGON BL RC Healing abutment Ø 7.0 mm GH 4.0 mm
• Version Model Number: 22123
• Catalog Number: 22123
• 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: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de
• Phone: +492173398000
• Email: info@dental-ratio.de

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EDRS221231 [Primary]

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

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

[EDRS221231]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-02-14
• Device Publish Date: 2017-01-27

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