Primary Device ID | 00619498020034 |
NIH Device Record Key | b6adae0e-fcc9-478e-8fbb-b166f9ad5067 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Narval CC |
Version Model Number | 200047 |
Catalog Number | 200047 |
Company DUNS | 147450258 |
Company Name | RESMED MOTOR TECHNOLOGIES INC. |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | 800-424-0737 |
reception@resmed.com | |
Phone | 800-424-0737 |
reception@resmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00619498020034 [Primary] |
LQZ | Device, Jaw Repositioning |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-05 |
00619498020041 | Mandibular Repositioning Device |
00619498020034 | Connecting Rods Pack - Upper range |
00619498020027 | Connecting Rods Pack - Lower Range |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NARVAL CC 85489200 not registered Dead/Abandoned |
ResMed SAS 2011-12-07 |