Ritter Implants Dental System

GUDID ERITNLCOD3041

Ritter Implants GmbH & Co. KG

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Primary Device ID	ERITNLCOD3041
NIH Device Record Key	edd6ec16-8344-4de7-b387-3e81e9db71fd
Commercial Distribution Status	In Commercial Distribution
Brand Name	Ritter Implants Dental System
Version Model Number	NL-COD-30-4
Company DUNS	342602800
Company Name	Ritter Implants GmbH & Co. KG
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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	ERITNLCOD3041 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K180183

FDA Product Code

NHA	Abutment, Implant, Dental, Endosseous