Primary Device ID | 20862478000456 |
NIH Device Record Key | 34dbd79a-6183-49ed-ad63-950d6bb94f35 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SSO2 Catheter |
Version Model Number | SSO2 - 4.5 |
Company DUNS | 835420894 |
Company Name | THEROX, 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 | true |
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 | 949-757-1999 |
customerservice@therox.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00862478000452 [Primary] |
GS1 | 10862478000459 [Package] Contains: 00862478000452 Package: Single pack carton [1 Units] In Commercial Distribution |
GS1 | 20862478000456 [Package] Contains: 00862478000452 Package: Five pack carton [5 Units] In Commercial Distribution |
MWG | System, Oxygen, Aqueous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-08-16 |
Device Publish Date | 2019-08-08 |
20862478000463 | The TherOx DownStream System, is indicated for the preparation and delivery of SuperSaturated Ox |
20862478000456 | The TherOx DownStream System, is indicated for the preparation and delivery of SuperSaturated Ox |
20862478000449 | The TherOx DownStream System, is indicated for the preparation and delivery of SuperSaturated Ox |
20862478000432 | The TherOx DownStream System, is indicated for the preparation and delivery of SuperSaturated Ox |