Primary Device ID | 16946159504017 |
NIH Device Record Key | a9c27e78-ccc7-4e69-a315-94f98d55a3a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Willis the Whale |
Version Model Number | 1133818 |
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 | 06946159504010 [Primary] |
GS1 | 16946159504017 [Package] Contains: 06946159504010 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 |
16946159504024 | 1133796 |
16946159504017 | 1133818 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WILLIS THE WHALE 79215832 5516126 Live/Registered |
Koninklijke Philips N.V. 2017-07-07 |