OKTAGON BL RC Basic screw, L 7.5 mm for cementable abutment 22120

GUDID EDRS221201

BL RC Basic screw, L 7.5 mm for cementable abutment for OKTAGON Dental Implant BL RC

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Dental implant suprastructure, permanent, preformed

• Primary Device ID: EDRS221201
• NIH Device Record Key: e7518940-e383-491f-aa2f-087b2f8bebc0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OKTAGON BL RC Basic screw, L 7.5 mm for cementable abutment
• Version Model Number: 22120
• Catalog Number: 22120
• 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	EDRS221201 [Primary]
HIBCC	EDRS221209 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143539

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

[EDRS221201]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-08-30

On-Brand Devices [OKTAGON BL RC Basic screw, L 7.5 mm for cementable abutment]

• EDRS221201: BL RC Basic screw, L 7.5 mm for cementable abutment for OKTAGON Dental Implant BL RC
• E0HM221201: BL RC Basic screw, L 7.5 mm for cementable abutment for OKTAGON Dental Implant BL RC