Primary Device ID | 10816317023017 |
NIH Device Record Key | 54414bed-4b54-4e64-9a23-b3f6e8a752de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ethox |
Version Model Number | RM-4010H |
Company DUNS | 100439103 |
Company Name | RENU MEDICAL, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816317023010 [Primary] |
GS1 | 10816317023017 [Package] Contains: 00816317023010 Package: Case [5 Units] In Commercial Distribution |
KZD | Infusor, Pressure, For I.V. Bags |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-05 |
Device Publish Date | 2023-06-27 |
10816317023017 | Ethox Pressure Infusor Bag with Hook 1000cc |
10816317023000 | Ethox Pressure Infusor Bag with Hook 500cc |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ETHOX 86005671 4524762 Live/Registered |
Ethox Chemicals, LLC 2013-07-09 |
ETHOX 75183274 2091414 Live/Registered |
SUNMED HOLDINGS, LLC 1996-10-17 |
ETHOX 75182990 2123310 Live/Registered |
VENTLAB HOLDINGS, LLC 1996-10-17 |
ETHOX 74145930 1695734 Live/Registered |
VENTLAB HOLDINGS, LLC 1991-03-11 |
ETHOX 73075326 1046293 Dead/Expired |
Ethox Corp. 1976-01-26 |