CONELOG® Bite registration post C2141.5000

GUDID E219C214150001

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

Device Issuing Agency	Device ID
HIBCC	E219C214150001 [Primary]

NDP	Accessories, Implant, Dental, Endosseous

Steralize Prior To Use	false
Device Is Sterile	true

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

Mark Image Registration \| Serial	Company Trademark Application Date
CONELOG 79032509 3527657 Live/Registered	Camlog Biotechnologies GmbH 2006-11-17