FDA UDI In Commercial Distribution 🇺🇸 United States

NARVAL CC

DI: 03760287780022 · Model: 200002 · RESMED SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NARVAL CC
Primary DI
03760287780022
Version / Model
200002
Company Name
RESMED SA
Labeler DUNS
383473204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-18
Public Version
1
Public Version Date
2018-11-19
Public Version Status
New
Public Device Record Key
ea2dec3c-48ae-4f44-a18e-26faa5439ba1

Device Description

The Narval CC mandibular repositioning device is a removable intraoral device used for the treatment of snoring and Obstructive Sleep Apnea (OSA). Similarly to other mandibular repositioning device, the Narval CC functions by advancing the lower jaw (mandible) in a forward position during sleep. This acts to increase the patient's pharyngeal space, improving their ability to exchange air and reducing their tendency to snore.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LQZ Device, Jaw Repositioning

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 03760287780022

Premarket Submissions

Submission Number Supplement Number
K113201 000