Primary Device ID | 00850033705072 |
NIH Device Record Key | ac8e1f51-8658-4337-b421-77fb3d6c4551 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Co2mmander® ELITE |
Version Model Number | COM915 |
Catalog Number | COM915 |
Company DUNS | 965605210 |
Company Name | Angioadvancements, LLC |
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 | true |
Manufacturing Date | true |
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 | 00850033705072 [Primary] |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-22 |
Device Publish Date | 2022-08-12 |
00850033705003 | Regulator, Pressure, Gas Cylinder - Co2mmander CO2 Delivery System |
00850033705072 | Co2mmander® ELITE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CO2MMANDER 87394244 5316073 Live/Registered |
Frank L. Levy 2017-03-31 |
CO2MMANDER 77578551 3819118 Live/Registered |
Frank L. Levy 2008-09-25 |