| Primary Device ID | 16946159501023 |
| NIH Device Record Key | 35e64580-4449-4c84-9d4d-7088954e565c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sami the Seal |
| Version Model Number | 1093270 |
| 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 | 06946159501026 [Primary] |
| GS1 | 16946159501023 [Package] Contains: 06946159501026 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 |