CAMLOG® Bite registration post J2141.5000

GUDID E219J214150001

Dental implant suprastructure, temporary, preformed, single-use

Primary Device ID	E219J214150001
NIH Device Record Key	d2ffadcc-02ed-4b95-833b-2fe70aa042e2
Commercial Distribution Status	In Commercial Distribution
Brand Name	CAMLOG® Bite registration post
Version Model Number	J2141.5000
Catalog Number	J2141.5000
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	E219J214150001 [Primary]

NDP	Accessories, Implant, Dental, Endosseous

Steralize Prior To Use	false
Device Is Sterile	true

E219J214150001	CAMLOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 5.0 mm, prosth
E219J214143001	CAMLOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 4.3 mm, prosth
E219J214138001	CAMLOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 3.8 mm, prosth
E219J214133001	CAMLOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 3.3 mm, prosth

Mark Image Registration \| Serial	Company Trademark Application Date
CAMLOG 79003716 3055564 Live/Registered	Camlog Biotechnologies GmbH 2004-05-14