Blue EF Series,Retainer

GUDID 06972677871754

Modern Dental Laboratory (DG) Co., Ltd.

Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis

Primary Device ID	06972677871754
NIH Device Record Key	af0a0fe3-bd7b-46e9-ae8b-de1b73ea73bd
Commercial Distribution Status	In Commercial Distribution
Brand Name	Blue EF Series,Retainer
Version Model Number	174
Company DUNS	551746187
Company Name	Modern Dental Laboratory (DG) Co., Ltd.
Device Count	2
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	false
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	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972677871747 [Primary]
GS1	06972677871754 [Unit of Use]

FDA Product Code

LRK	Device, Anti-Snoring