CCM Cylinder MCCM 5005H

GUDID 08800049251201

DIO Corporation

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

Primary Device ID	08800049251201
NIH Device Record Key	0c56ed38-4e37-4665-a17b-1f181be2bab9
Commercial Distribution Status	In Commercial Distribution
Brand Name	CCM Cylinder
Version Model Number	MCCM 5005H
Catalog Number	MCCM 5005H
Company DUNS	631085206
Company Name	DIO Corporation
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	true
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 Identifiers

Device Issuing Agency	Device ID
GS1	08800049251201 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K182194

FDA Product Code

NHA	Abutment, Implant, Dental, Endosseous