Primary Device ID | 16946159501061 |
NIH Device Record Key | 5de2b721-a4b2-4e19-bfa2-eed6924e02fe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sami the Seal |
Version Model Number | 1082731 |
Company DUNS | 421290561 |
Company Name | VEGA 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 | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 06946159501064 [Primary] |
GS1 | 16946159501061 [Package] Contains: 06946159501064 Package: [6 Units] In Commercial Distribution |
CAF | Nebulizer (Direct Patient Interface) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-07-02 |
Device Publish Date | 2018-06-01 |
16946159501092 | 1136955 |
16946159501085 | 1119462 |
16946159501078 | 1114373 |
16946159501061 | 1082731 |
16946159501054 | 1082456 |
16946159501047 | 1093268 |
16946159501030 | 1093237 |
16946159501023 | 1093270 |
06946159501019 | 1093235 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SAMI THE SEAL 79147188 4857178 Live/Registered |
Koninklijke Philips N.V. 2014-04-03 |
SAMI THE SEAL 78855335 3684556 Dead/Cancelled |
RIC Investments, LLC 2006-04-06 |