CONELOG® Bite registration post C2141.5000

GUDID E219C214150001

CONELOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 5.0 mm, prosthetic height 8.1 mm, titanium alloy/PBT, sterile

ALTATEC GmbH

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: E219C214150001
• NIH Device Record Key: 46eaa34d-046d-47fc-a065-d97d2debc332
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONELOG® Bite registration post
• Version Model Number: C2141.5000
• Catalog Number: C2141.5000
• Company DUNS: 322018193
• Company Name: ALTATEC GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: true
• 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: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E219C214150001 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-26
• Device Publish Date: 2023-12-18

On-Brand Devices [CONELOG® Bite registration post]

• E219C214150001: CONELOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 5.0 mm, prost
• E219C214143001: CONELOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 4.3 mm, prost
• E219C214138001: CONELOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 3.8 mm, prost
• E219C214133001: CONELOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 3.3 mm, prost