Primary Device ID | 00709078002397 |
NIH Device Record Key | f9ba0904-968f-4607-a910-2abf70703f3a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VIBRALUNG® |
Version Model Number | 9500D |
Company DUNS | 092673953 |
Company Name | WESTMED, 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 | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 93 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 93 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 93 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 93 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00709078002397 [Primary] |
BYI | Percussor, Powered-Electric |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-04-17 |
10709078002417 | VIBRALUNG® HHT Hanger |
00709078002403 | Demo User Kit with Travel Bag, VIBRALUNG® |
00709078002397 | Demo Treatment Control Unit Assembly, VIBRALUNG® Acoustical |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VIBRALUNG 78405637 3389688 Live/Registered |
VibraLung, Inc. 2004-04-21 |